NABL 100

National Accreditation Board for

Testing and Calibration
Laboratories (NABL)

General Information Brochure

Issue Date: 04-June-2019

 Contents

SI. Contents Pages

Contents
1. Conformity Assessment 2

2. Benefits of Accreditation 5

3. About NABL 7

4. International Linkages 10

5. Scope of NABL Accreditation 11

6. Preparing for Accreditation 13

7. Eligibility for Accreditation 14

8. Accreditation Procedure 15

9. Integrated Assessment of Testing Laboratories by NABL & 20

Regulatory Body (ies)
10. Quality Assurance Scheme for Basic Composite Medical 23
Laboratories (Entry Level)
11. Maintaining Accreditation 24

12. Surveillance and Re-assessment 25

13. Appeals and Complaints 26
14. Rights and Obligations of CABs 27

15. Rights and Duties of NABL 29

16. NABL Finance and NABL Fee Structure 31
17. Modes of Payment 38

18. NABL Publications 39

Contact Details 41

National Accreditation Board for Testing and Calibration Laboratories 1/41

1. Conformity Assessment

International Standard ISO/IEC 17000 defines Conformity Assessment as a “Demonstration that

specified requirements related to a product, process, system, person or body are fulfilled.”
Conformity Assessment procedures, such as testing / calibration, inspection and certification,
offers assurance that products fulfill the requirements specified in regulation and standards.

Each organization must decide which type of conformity assessment is necessary for which
purpose. This decision should be based on an assessment of the risk involved with a particular
product or process, and on an understanding of the impact the associated costs and benefits
will have on achievable development.

Successive reviews of the WTO/TBT agreement have noted the usefulness of ISO/IEC
conformity assessment standards and guide in harmonizing the conformity assessment practice
and as benchmarks for the technical competence of assessment bodies, thus enhancing the
credibility and confidence in their results. ISO/IEC conformity assessment work therefore helps
to overcome technical trade barrier.

Accreditation is the third-party attestation related to a conformity assessment body conveying

the formal demonstration of its competence to carry out specific conformity assessment task.
Conformity Assessment Body (CAB) is a body which includes Testing including Medical
Laboratory, Calibration Laboratory, Proficiency Testing Provider and Reference Material
Producers.

Laboratory accreditation is a procedure by which an authoritative body gives formal recognition

of technical competence for specific tests/ measurements, based on third party assessment and
following international standard.

The general requirements for laboratories or other organizations, to be considered competent to

carry out sampling, testing (other than medical) and calibration are specified in the International
Standard ISO/IEC 17025:2005 or ISO/IEC 17025:2017.

Another very important area under testing, which plays a vital role in human health, is medical /
clinical diagnostic testing. Requirements for quality and competence to carry out sampling and
testing in medical field are specified in the International Standard ISO 15189:2012. NABL also
grants accreditation to Medical Imaging- Conformity Assessment Body (MI-CAB) based on ISO
15189:2012.

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Further, to strengthen the pre-examination process performed in sample Collection Centres /
Facility(ies), NABL also recognizes these Sample Collection Centres / Facility(ies) declared by
its associated accredited medical laboratories. NABL recognition of Sample Collection Centres/
Facility (ies) (SCF) declared by medical testing laboratories, is of paramount significance in
ensuring the quality services rendered by the Sample Collection Centres/ Facilities (SCF). The
assessment of all declared Sample Collection Centres/ Facility(ies) will ensure integrity of
samples and better control on pre-examination processes as quality of test results largely
depends on these processes. Moreover, this will also enhance the confidence of Sample
Collection Centres / Facility (ies) and accord due recognition to these Centres / Facilities (SCF).
The laboratory shall be responsible for the operation of the recognized Sample Collection
Centres / Facility (ies).

Proficiency Testing is the use of inter-laboratory comparison for determining the performance of
individual laboratories for specific tests. Participation in proficiency testing programmes provides
laboratories with an objective means of assessing and demonstrating the reliability of data they
are producing. The International Standard ISO/IEC 17043:2010 provides a consistent basis for
all interested parties to determine the competence of organizations that provide proficiency
testing.

Certified Reference Materials (CRMs) are 'controls' or standards used to check the quality and
metrological traceability of products, to validate analytical measurement methods, or for the
calibration of instruments. The reference material producer is fully responsible for project
planning and management, assignment of and decision on property values and relevant
uncertainties, authorization of property values and issue of the certificate and other statement
for the reference materials it produces. ISO 17034:2016 specifies General Requirements in
accordance with which a reference material producer has to demonstrate that it operates, if it is
to be recognized as competent to carry out the production of reference materials.

In the current global scenario, an essential pre -requisite of trade is that any product or service
accepted formally in one economy must also be free to circulate in other economies without
having to undergo extensive re-testing. WTO recognizes that non-acceptance of test results and
measurement data is a Technical Barrier to Trade. Global sourcing of components calls for
equivalence of measurement, which can be facilitated by a chain of accredited CABs.
Accreditation is considered as the first essential step for facilitating mutual acceptance of test

National Accreditation Board for Testing and Calibration Laboratories 3/41

results and measurement data.

Confidence in accreditation is obtained by a transparent system of control over the accredited

CABs and an assurance given by the accreditation body that the accredited CAB fulfils the
accreditation criteria, at all times.

Accredited CABs can objectively state conformance of product or service to the specified
requirements. It is important for the purchaser, regulator, government and public to be able to
identify the accredited CABs.

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2. Benefits of Accreditation

Formal recognition of competence of a laboratory by an Accreditation body in accordance with

international criteria has many advantages:
 Increased confidence in Testing/ Calibration Reports issued by the laboratory.
 Better control of laboratory operations and feedback to laboratories as to whether they
have sound Quality Assurance System and are technically competent.
 Potential increase in business due to enhanced customer confidence and satisfaction.
 Customers can search and identify the laboratories accredited by NABL for their specific
requirements from the NABL Web -site or Directory of Accredited Laboratories.
 Users of accredited laboratories enjoy greater access for their products, in both domestic
and international markets.
 Savings in terms of time and money due to reduction or elimination of the need for re-
testing of products.

The benefits of proficiency testing are widely recognized. These include:

 Comparison of a facility’s performance with that of other participating (peer) facilities

 Monitoring of a long-term facility performance
 Improvement in the performance of tests/calibrations following investigation and
identification of the cause(s) of unsatisfactory PT performance, and the introduction of
corrective action to prevent re-occurrence
 Staff education, training and competence monitoring
 Evaluation of methods, including the establishment of method precision and accuracy
 Estimation of measurement uncertainty
 Contribution to the facility’s overall risk management system
 Confidence building with interested parties, e.g. customers, accreditation bodies,
regulators, specifiers.

Proficiency testing providers play an important role in the value chain for assurance of products
and services. Being an accredited PTP gives the organization credibility for their PT services.

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Formal recognition of competence of a RMP by an Accreditation body in accordance with
international criteria has many advantages

 Accreditation is an effective marketing tool for RMPs.

 Accreditation provides assurance that the accredited RMPs are competent to produce
the RMs as listed in the scope of accreditation.
 It provides confidence to RM users that the reference materials (RMs), and certified
reference materials (CRMs) in particular, are produced according to technically valid and
internationally recognized principles, and fitted for the intended uses.
 These uses include the assessment of precision and trueness of measurement methods,
quality control, assigning values to materials, calibration, and the establishment of
conventional scales. This eliminates the needs of the users to evaluate the quality of the
RMs themselves.
 RMs are used globally. Many economies around the world have accreditation bodies
offering accreditation to RMPs. These accreditation bodies have adopted ISO Guide 34:
2009 / ISO 17034:2016 as the criteria for RMP accreditation. This has helped
economies to adopt a uniform approach to determining RMP competence. This uniform
approach allows accreditation bodies in different economies to establish arrangements
among themselves, based on mutual evaluation and acceptance of each other’s RMP
accreditation systems.

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3. About NABL

NABL is a constituent Board of Quality Council of India (QCI). QCI is a registered society under
the Societies Registration Act, 1860. Department for Promotion of Industry and Internal Trade,
Ministry of Commerce and Industry, Government of India is the nodal Department for QCI.

NABL has been established with the objective of providing Government, Industry Associations
and Industry in general with a scheme of Conformity Assessment Body’s accreditation which
involves third-party assessment of the technical competence of testing including medical and
calibration laboratories, proficiency testing providers and reference material producers.

The laboratory accreditation services to testing and calibration laboratories are provided in
accordance with ISO/ IEC 17025: 2005 or ISO/IEC 17025:2017 ‘General Requirements for the
Competence of Testing and Calibration Laboratories’ and ISO 15189: 2012 ‘Medical
laboratories -- Requirements for quality and competence’ The accreditation to Proficiency
testing providers are based on ISO/IEC 17043 :2010 “Conformity assessment -- General
requirements for proficiency testing” and to Reference Material Producers based on ISO
17034:2016 - General requirements for the competence of reference material producers ”The
fields, disciplines and groups for which the accreditation services are offered are listed in ‘Scope
of NABL Accreditation’.

NABL offers accreditation services in a non-discriminatory manner. These services are

accessible to all testing including medical and calibration laboratories, proficiency testing
providers and reference material producers in India and other countries in the region, regardless
of the size of the applicant CAB or its membership of any association or group or number of
CABs already accredited by NABL.

NABL has established its accreditation system in accordance with ISO/ IEC 17011: 2017
‘Conformity Assessment –Requirements for Accreditation bodies accrediting conformity
assessment bodies’. NABL accreditation system also takes note of the requirements of Mutual
Recognition Arrangements (MRAs) of which NABL is a member.

NABL publishes documents for the CABs, Assessors and its own use. A list of NABL documents
is given at the end of this document. All NABL documents meant for the use by persons outside
NABL, are available on NABL website www.nabl-india.org, free of cost.

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Organization Structure of NABL

The organization structure of NABL has been designed to meet the requirements of an effective
and efficient accreditation system.

The Apex body in NABL organization is the NABL Board. The Board provides policy, guidelines
and direction to NABL. CEO, NABL is the Member Secretary of the NABL Board. NABL
Secretariat comprises of Chief Executive Officer (CEO), Director, Joint Director, Deputy
Director, Assistant Director, Quality Manager, Complaints Manager, Appeals Officer,
Accreditation Officers, Administration and support staff. The CEO, NABL is responsible for
administering and managing the day to day operations of NABL Secretariat.

The organization chart (Technical) of NABL is given below –

NABL Board

Chief Executive Officer

(CEO)

Impartiality Committee

Director Director Director

Quality Cell (Testing, Appeals Officer
(Calibration) (Medical)
PTP, RMP)

Marketing & Strategy Complaints Manager

International Affairs Training & Assessors

JD JD JD JD JD JD JD Monitoring Committees
(Gr.-C1) (Gr.-T1) (Gr.-T2) (Gr.-T3) (Gr.-Tn) (Gr.-M1) (Gr.-M2)

Accreditation Committees

DD/AD/Officers DD/AD/Officers DD/AD/Officers

Technical Committees

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NABL operates its accreditation process through empanelled Lead Assessors and Technical
Assessors covering all fields and disciplines as specified in the scope of NABL. All Lead
Assessor and Technical Assessors are personnel having considerable experience in CAB
activities. They are trained by NABL as per the relevant international accreditation criteria and
subsequently empanelled as assessors/ lead assessors through contractual agreements.

Recommendations of Accreditation Committee form the basis for accreditation decisions.

Membership of accreditation committees is drawn from NMIs and standards bodies,
experienced assessors (including those from accredited CABs), academic institutions, important
professional bodies, regulatory agencies/ bodies etc. The members of the Accreditation
Committee are selected on the basis of their technical knowledge and familiarity with
accreditation process. However, care is taken while selecting composition of an Accreditation
Committee that expertise in all areas covered under the committee is available and no single
group or organization pre-dominates the committee.

The formulation of technical/ specific guidelines and other similar tasks is derived from various
ad-hoc technical committees set up for the purpose. Composition of Technical Committee is
mainly driven by the purpose for which the committee is set up. For multi-disciplinary fields or in
areas where two or more fields overlap, care is taken to include members from relevant fields so
that a balanced view emerges. Committee members are drawn from different organizations that
form the spectrum of interested parties.

Related bodies

The National Metrological Institutes (NMIs) namely National Physical Laboratory (NPL) and
Bhabha Atomic Research Centre (BARC); the Standards Bodies namely Bureau of Indian
Standards (BIS) and Standardization, Testing and Quality Certification (STQC), Council for
Industrial and Scientific Research (CSIR), the other Boards of Quality Council of India (QCI),
the other organizations under nodal department of QCI i.e. Department for Promotion of
Industry and Internal Trade, the other Departments / organizations under nodal Ministry i.e.
Ministry of Industry and Commerce are the bodies related to NABL. Due care is taken to
determine and avoid potential for conflict of interest from the activities of the related bodies in
the operation of NABL.

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4. International Linkages

NABL maintains linkages with the international bodies like International Laboratory Accreditation
Co-operation (ILAC) and Asia Pacific Accreditation Co-operation (APAC). NABL is a full
member of ILAC and APAC and regularly takes part in their meetings. More information on
these international co operations can be obtained from their web-sites www.ilac.org and
www.apac-accreditation.org respectively.

NABL is signatory to ILAC as well as APAC Mutual Recognition Arrangements (MRA) for
accreditation of Testing including Medical and Calibration laboratories, which is based on
mutual evaluation and acceptance of other MRA Partner accreditation systems. Such
international arrangements facilitate acceptance of test/ calibration results between countries
which MRA partners represent. NABL is also signatory to APAC MRA for accreditation of
Proficiency Testing Providers (PTP) and Reference Material Producers (RMP)

The information on ILAC and APAC Mutual Recognition Arrangements (MRA s) is available at
NABL web-site. On request from the laboratories or their users, a copy of ILAC/ APAC MRA is
provided.

In order to achieve the objective of the acceptance of test/ calibration data across the borders,
NABL operates and is committed to update its accreditation system as per international norms.
NABL operations conform to ISO/ IEC 17011: 2017.

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5. Scope of NABL Accreditation

NABL Accreditation is currently given in the following fields and disciplines. The multi-
disciplinary CABs shall have to apply in relevant discipline separately depending upon to which
discipline the scope belongs.

TESTING FIELD
 Chemical
 Biological
 Mechanical
 Electrical
 Electronics
 Fluid Flow
 Forensic
 Non Destructive (NDT)
 Photometry
 Radiological

CALIBRATION FIELD
 Mechanical
 Electro Technical
 Fluid Flow
 Thermal
 Optical
 Medical Devices
 Radiological

MEDICAL FIELD
 Clinical Biochemistry
 Clinical Pathology
 Haematology & Immunohaematology
 Microbiology & Serology
 Histopathology
 Cytopathology
 Genetics
 Nuclear Medicine (In-vitro tests only)

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Medical Imaging- Conformity Assessment Bodies (MI-CAB)
 Projectional Radiography & Fluoroscopy
a. X-Ray, Bone Densitometry (DEXA), Dental X-Ray-OPG, Mammography etc.
b. Fluoroscopy
 Computed Tomography (CT)
 Magnetic Resonance Imaging (MRI)
 Ultrasound and Colour Doppler
 Nuclear Medicine
a. SPECT
b. PET CT
c. PET MRI
 *Basic Diagnostic Interventional Radiology Procedures
(Image guided Core Biopsy and / or Needle Aspiration e.g. Fine Needle Aspiration Cytology)
*For only such IR procedures that will be carried out by Radiologists

PROFICIENCY TESTING PROVIDERS (PTP)

 Testing
 Calibration
 Medical
 Inspection

REFERENCE MATERIAL PRODUCERS (RMP)

 Chemical Composition
 Biological & Clinical Properties
 Physical Properties
 Engineering Properties
 Miscellaneous Properties

For classification of product groups in each field, refer NABL 120 for Testing & Calibration,
NABL 180 for PTP & NABL 191 for RMP.

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6. Preparing for Accreditation

Once the CAB decides to seek NABL accreditation, it should make a definite plan of action for
obtaining accreditation and nominate a responsible person to co-ordinate all activities related to
seeking accreditation. The person nominated should be familiar with CAB’s existing quality
system.

A list of NABL external documents is given at the end of this document and is also available on
NABL website under Publications – Accreditation Documents. The CAB should get fully
acquainted with relevant NABL documents and understand the assessment procedure and
methodology for filing the on-line application. NABL only accepts online application and do not
entertain any applications in hard copy (kindly refer website www.nabl-india.org).

CAB needs to ascertain the status of its existing quality system and technical competence with
regards to the requirement of ISO/ IEC 17025:2017 or ISO 15189:2012 or ISO/IEC 17043:2010
or ISO 17034:2016 whichever is relevant and requirements of NABL. The questions the CAB
needs to address are:

 Does the CAB have a quality management system? 


 If yes, is the quality management system documented and effective? 

 If no, what are the corrective steps needed? 

It must be remembered that CAB has to prepare a Management system document/ quality
manual, which has to be supplemented by a set of other documents like procedural manuals,
work instructions etc. Requirements of the applicable standard and relevant NABL specific
criteria (wherever applicable) should be discussed amongst concerned staff of the CAB. This
will enable them to understand their strengths and weaknesses.

For preparing the Management system document/ quality manual or verifying its contents, the
CAB may get its technical personnel trained in training programs on quality management
system for CAB personnel organized by various institutes. The proposed person responsible for
quality management system shall have undergone 4-days formal training on management
system and internal audit based on relevant standard or any other equivalent training on the
relevant standard in case of overseas CABs (Kindly refer NABL 165 for the training
requirement).

The CAB must ensure that the procedures described in the Management system document/
quality manual and other documents are being implemented.

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7. Eligibility for Accreditation

The applicant CAB must comply with all clauses of ISO/IEC 17025:2005/ ISO/IEC 17025:2017
or ISO 15189: 2012 or ISO/IEC 17043:2010 or ISO 17034:2016 whichever is applicable. The
applicant CAB must also comply with the relevant NABL specific criteria (wherever applicable).

In case the laboratory performs site testing/ calibration, it must also comply with NABL 130
‘Specific criteria for site testing and site calibration laboratories.

The applicant CAB must have participated satisfactorily in the proficiency testing program,
wherever applicable, conducted by NABL/ APAC or any other national or international
accredited/ recognized PT provider. If no suitable PT program is available the CAB can initiate
an inter-laboratory comparison with adequate number of accredited laboratories. The minimum
stipulated participation for laboratories is one parameter/ type of test/ calibration per discipline,
prior to grant of accreditation and an on-going program as per NABL 163. The satisfactory
performance shall be defined in term of z-score and En number respectively or any other
acceptable internationally accepted method. For unsatisfactory performance, the CAB is to take
corrective action and inform NABL. ISO/ IEC 17043, NABL 163 and NABL 164 give details of
proficiency testing.

The applicant CAB must have conducted at least one internal audit and a management review
before the submission of application. ISO 19011 ‘Guidelines for auditing management systems'
and NABL 161 ‘Guide for Internal Audit and Management Review for CABs’ provides the
necessary guidance for CABs.

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8. Accreditation Procedure

Application for Accreditation

(by CAB)

Acknowledgement & Scrutiny of

Application (by NABL Secretariat)
Information
to
Document review (by Lead Assessor) CAB

Pre-Assessment of CAB and

Optional (by Lead Assessor)

Final Assessment of CAB Necessary

(by Assessment Team) Corrective
Action
by
Scrutiny of Assessment Report CAB
(by NABL Secretariat)

Recommendations for Accreditation

(by Accreditation Committee)

Approval for Accreditation

(by Chairman, NABL)

Issue of Accreditation Certificate

(by NABL Secretariat)

Flow Diagram of Accreditation Process

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 Application for Accreditation

CABs are required to apply through NABL Web Portal (through website www.nabl-india.org) to
NABL in prescribed application form (NABL 151, NABL 152, NABL 153) for Testing
including Medical along with associated Sample Collection Centre/ Facilities (SCF) / Calibration
Laboratories which should describe the management system in accordance with ISO/IEC
17025: 2017 or ISO 15189: 2012. The application fees shall be accompanied with prescribed
application fee as detailed in NABL 100.

CABs seeking accreditation for Medical Imaging- Conformity Assessment Body (MI-CAB) as per
ISO 15189:2012, are required to apply in prescribed application form NABL 156.

However, CABs are required to apply to NABL in prescribed application form (NABL 180 and
NABL 190) for Proficiency Testing Providers & Reference Material Producers in one copy along
with one copy of the Manual of the CAB which should describe the management system in
accordance with ISO/IEC 17043: 2010 or ISO 17034: 2016 whichever is applicable. The
application shall be accompanied with prescribed application fee as detailed in NABL 100. A
signed copy of NABL 131 shall also be submitted along with the application.

CAB has to take special care in filling the scope of accreditation/ uploading on the Web Portal
for which the CAB wishes to apply. In case, the CAB finds any clause (in part or full) not
applicable to the CAB, it is expected to furnish the reasons.

Acknowledgement and Registration of Application

NABL Secretariat through Web Portal, on receipt of online application form along with
Management system document / quality manual and the fees, send an acknowledgement with a
unique ID number to the CAB. The unique ID of the CAB will be used for further
correspondence with the CAB. After scrutiny of application for its completeness in all respects,
NABL Secretariat may ask for additional information/ clarification(s) at this stage, if found
necessary.

Appointment of Lead Assessor

NABL secretariat appoints a Lead assessor from the list of empanelled assessors. The lead
assessor does the document review on behalf of NABL and submits the report to NABL
secretariat.

Document Review

The preliminary document review of the application and management system document/
quality manual submitted by the CAB is carried out by NABL Secretariat whereas the detailed
National Accreditation Board for Testing and Calibration Laboratories 16/41
review is carried out by Lead Assessor.

The lead assessor informs NABL regarding the document review, indicating inadequacies (if
any). The CAB amends the relevant documents and also implements the management system
accordingly.

Pre-Assessment

In case there are no inadequacies in the document review after satisfactory corrective action
by the CAB, a pre -assessment of the CAB is conducted by lead assessor appointed by NABL.
Since Pre-assessment is optional, CAB shall express its willingness in writing to undergo the
same. The CAB must ensure their preparedness by carrying out an internal audit and a
management review before the pre -assessment.

The pre-assessment of the CAB is conducted to:

a. evaluate non-conformities (if any) in the implementation of the quality system.

b. assess the degree of preparedness of the CAB for the assessment

c. determine the number of assessors required in various fields based on the scope of
accreditation, number of key locations to be visited etc.

The lead assessor submits a pre-assessment report to NABL Secretariat with a copy to the
CAB. The CAB takes corrective actions on the non-conformities raised on the documented
management system and its implementation and submits a report to NABL Secretariat.

Assessment

After the CAB has taken corrective actions, NABL proposes constitution of an assessment
team. The team includes the lead assessor (generally same who is already appointed for pre-
assessment), the technical assessor(s)/ expert(s) in order to cover various fields within the
scope of accreditation sought. NABL may also nominate an observer. NABL seeks CAB’s
acceptance for the proposed assessment team and the CAB is free not to accept one or more
members of the proposed assessment team by giving specific reason(s) for their non -
acceptance.

After the constitution of assessment team is finalized, NABL fixes dates for on-site
assessment in consultation with the CAB, the lead assessor and technical assessor(s)/
expert(s).

The assessment team reviews the CAB ’s documented management system and verifies its
compliance with the requirements of ISO/ IEC 17025: 2005/ ISO/IEC 17025:2017 or ISO

National Accreditation Board for Testing and Calibration Laboratories 17/41

15189: 2012 or ISO/IEC 17043:2010 or ISO 17034:2016 whichever is applicable and relevant
specific criteria (wherever applicable) and other NABL policies. The documented
Management system, SOPs, work instructions, test methods etc. are assessed for their
implementation and effectiveness. The CAB’s technical competence to perform specific tasks
is also evaluated.

The assessment report contains the evaluation of technical manpower, all relevant material
examined, test witnessed including those of replicate testing/ measurement, compliance to
ISO/ IEC 17025: 2005/ ISO/IEC 17025:2017 or ISO 15189: 2012 or ISO/IEC 17043:2010 or
ISO 17034:2016 whichever is applicable and relevant NABL specific criteria. The non-
conformities if identified are reported in the assessment report. It also provides a
recommendation towards grant of accreditation or otherwise. The report prepared by the
assessment team is sent to NABL Secretariat. However, a copy of summary of assessment
report and copies of non-conformities if any, are provided to the CAB at the end of the
assessment visit.

Assessment of each declared Sample Collection Centre/ Facility (SCF) of a medical laboratory
will be done in each accreditation cycle. This may be done along with assessment of the
laboratory or separately as the case may be.

Scrutiny of Assessment Report

The assessment report is examined by NABL Secretariat and follow up action as required is
initiated. CAB has to take necessary corrective action on non - conformities/ concerns and
submit a report to NABL Secretariat within 30 days. NABL monitors the progress of closing of
non -conformities.

If any non-conformity is observed during the assessment of a Sample Collection Centre/

facility (SCF), the laboratory shall be asked to take corrective actions within 30 days time. In
case the laboratory fails to take corrective actions or there is a consistent system failure, an
appropriate and proportionate action against the laboratory will be taken.

Accreditation Committee

After satisfactory corrective action by the CAB, the Accreditation Committee examines the
assessment report, additional information received from the CAB and the consequent
verification, if any.

In case the Accreditation Committee finds deficiencies in the assessment report, the NABL
Secretariat obtains clarification from the Lead Assessor/ Assessor/ CAB concerned. In case

National Accreditation Board for Testing and Calibration Laboratories 18/41

everything is in order, the Accreditation Committee makes appropriate recommendations
regarding accreditation of the CAB to the Chairman, NABL.

All decisions taken by NABL regarding grant of accreditation are open to appeal by the CAB.
The appeal is to be addressed to the CEO, NABL.

Issue of Accreditation Certificate

When the recommendation results in the grant of accreditation, NABL issues an accreditation
certificate which has a unique number and QR Code, discipline, date of validity along with the
scope of accreditation.

The accreditation certificate for testing laboratory defines Discipline/ Group, product / Materials
of test, specific tests performed, test method/ specification against which tests are performed
and range of testing / limits of detection, wherever applicable.

The accreditation certificate for calibration laboratory defines Discipline/ Group, quantity
measured/ instrument, range/ frequency and Calibration and Measurement Capability (±) and
remarks.

The accreditation certificate for medical laboratory defines Discipline, / products/ material of
test, specific tests performed, test method, range of testing/ limit of detection, wherever
applicable and % CV. The annexure to the accreditation certificate will also contain the details
of recognized Sample Collection Centres/ Facilities associated.

The accreditation certificate for proficiency testing provider defines Proficiency Testing
scheme, Proficiency testing item, Analyte / Parameter / Test method.

The accreditation certificate for reference material producer defines Type of RM/CRM
Category/ Subcategory, reference material, properties to be certified (Analyte/ parameter or
etc.), range of property, assigned value uncertainty and best reference value capability (as
relevant) and characterization technique (s) used.

For site laboratory, tests/ calibrations performed at site are clearly identified in the scope of
accreditation while issuing the certificate.

The applicant CAB must make all payments due to NABL, before the accreditation
certificate(s) is/ are issued to them.

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9. Integrated Assessment of Testing Laboratories by NABL &
Regulatory Body (ies)

Integrated assessment is a unified approach to have a common assessment of laboratories for

NABL & Regulatory Body (ies) such as Export Inspection Council (EIC), Agricultural and
Processed Food Products Export Development Authority (APEDA), Indian Oilseeds and
Produce Export Promotion Council (IOPEPC), other commodity board (s) under the ambit of
Department of Commerce, Govt. of India and Food Safety & Standards Authority of India
(FSSAI) under Ministry of Health & Family Welfare, Govt. of India . This integrated approach will
ease laboratories in getting accredited by NABL in conjunction with the recognition/ approval by
the concerned Regulatory Body (ies) through a single assessment/ application.

Laboratories applying towards Accreditation and Recognition/Approval by NABL & Regulatory

Body (ies) under Integrated Assessment shall apply for all the parameters under applied
commodity/ product group as specified by the respective Regulatory Body (ies) in the prescribed
Application form; NABL 154, which is available on NABL website. Application with partial scope
for product/ matrix shall not be accepted and Recognition/Approval for partial scope shall not be
granted to the laboratories.

Followings are the framework:

o The requirements of NABL & Additional Requirements of Regulatory Body (ies) shall be
fulfilled by the Laboratories seeking Accreditation/ Recognition/ Approval through single
integrated assessment.

o Additional Requirements of Regulatory Body (ies) such as. EIC, APEDA, IOPEPC, other
Commodity Board(s) and FSSAI as defined in NABL 127: Procedure for Integrated
Assessment & Additional Requirements of Regulatory Body (ies) for testing laboratories
shall also be complied by the testing laboratories.

o The laboratory shall successfully participate in PT program as per NABL 163.

o Laboratories shall continuously participate in PT programs for the coverage of the scope in
a block of 4 years. Format for the submission of PT plan is available (Form 18 of NABL 163
available on NABL website).

National Accreditation Board for Testing and Calibration Laboratories 20/41

o Participation in PT program can be from National or International PT Provider who are
accredited as per ISO/IEC 17043. If accredited PT Providers are not available, then
participation in applicant PT provider is acceptable.

o When there is no PT program available nationally or internationally, the laboratory will

follow the requirements as defined by respective Regulatory Body’s additional requirement
document; NABL 127: Additional Requirements of Regulatory Body (ies) for testing
laboratories.

o Applicant/ accredited laboratories shall also comply with the requirements of PT

participation of concerned Regulatory Body as defined in NABL 127: Procedure for
Integrated Assessment & Additional Requirements of Regulatory Body (ies) for Integrated
Assessment.

o In case of unsatisfactory results of PT (Quantitative score |Z| ≥ 3) is scored, the same shall
be informed to NABL & other relevant Regulatory Body (ies) immediately. Laboratories
shall take appropriate corrective actions in case of poor performance in PT programs within
two months period.

o Apart from the above defined minimum requirements, lab shall abide by the PT
participation required by the respective Regulators, NABL & regional bodies like APAC.

o The duration of assessment shall be normally of 5 days depending upon the scope applied.
The assessment will cover compliance to ISO/IEC 17025, importing countries’
requirements, sampling and relevant additional requirement of EIC/ APEDA/ IOPEPC/
other Commodity Boards and FSSAI.

o Minimum one assessor per discipline shall be appointed for assessment and an expert to
assess the Sampling activity will also accompany the assessment team wherever
applicable.

o Accreditation and Recognition/ Approval of testing laboratories through integrated

assessment shall be subject to the annual Onsite surveillance visits to adjudge the
continued compliance to the said requirements. However, the Onsite surveillance will be
less comprehensive than re-assessment.

National Accreditation Board for Testing and Calibration Laboratories 21/41

o In case NABL or other authorities (who has granted approval under integrated assessment)
receives any complaint about any recognized/ accredited/ approved laboratory, a team
comprising of NABL, respective regulatory authority and any other technical expert as
deemed fit may be constituted and joint investigation may be carried out. In case, serious
violations are observed, then joint action including withdrawal/ suspension of accreditation
and Recognition and (or) approval shall be taken.

o All the test reports issued for the accredited scope under Integrated Assessment shall bear
NABL symbol in line with NABL 133; NABL Policy for Use of NABL symbol / Claim of
Accreditation by Accredited Conformity Assessment Bodies & NABL Accredited CAB
Combined ILAC MRA Mark.

National Accreditation Board for Testing and Calibration Laboratories 22/41

10. Quality Assurance Scheme for Basic Composite Medical Laboratories
(Entry Level)

For sensitizing the laboratories performing basic testing to quality practices and access to
quality health care for the majority of citizens especially those residing in villages, small towns,
NABL has launched voluntary scheme namely Quality Assurance Scheme for Basic Composite
Medical Laboratories (Entry Level). The criteria is based on the requirements enlisted in Gazette
notification dated 18th May, 2018 by MoHFW to amend Clinical Establishments (Central
Government) Rules, 2012. Components of competence assessment have been added for
assuring Quality and validity of test results.

This scheme of Basic Composite Medical Laboratories (Entry Level) is an independent quality
assurance scheme, which is not covered under APAC & ILAC MRA.

Interested laboratories are required to submit application and undergo third party assessment
by NABL. The assessment process is based on the checklist. Laboratories are required to pay
towards application fee, assessment charges and annual membership fee (Please refer section
of ‘NABL Finance and Fee Structures’ of this document for details). The laboratories will be
recognized for a period of two years. It is desired that subsequently the laboratories achieve
accreditation as per ISO 15189

The Scheme Documents, Application for Quality Assurance Scheme for Basic Composite
Laboratories (NABL 155) and Procedure for Quality Assurance Scheme for Basic Composite
Laboratories (NABL 128) are available on the website of NABL www.nabl-india.org.

National Accreditation Board for Testing and Calibration Laboratories 23/41

11. Maintaining Accreditation

Conformance to Applicable standards and NABL requirements

The accredited laboratories at all times shall conform to the requirements of ISO/IEC
17025:2017 or ISO 15189: 2012 or ISO/IEC 17043:2010 or ISO 17034:2016 whichever is
applicable and relevant specific criteria (wherever applicable) and NABL Policies.

NABL Terms and Conditions

The accredited CABs are required to comply at all times with the terms and conditions of
NABL given in NABL 131 ‘Terms & Conditions for obtaining and maintaining NABL
Accreditation’. The CABs are required to submit a signed copy of NABL 131 indicating their
willingness to abide by the terms and conditions given in NABL 131.

Modifications to the Accreditation Criteria

If the accreditation criteria are modified by ISO/ ILAC/ APAC/ NABL, the CAB is informed of
this giving a transition period of at least 6 months to align its operations in accordance with
the modified criteria.

Adverse decision against the laboratories

If the CAB at any point of time does not conform to the applicable standards and NABL
criteria; or does not maintain the NABL terms and conditions; or is not able to align itself to
the modified criteria, NABL may take adverse decision against the CAB like denial of
accreditation, scope reduction, abeyance, suspension or forced withdrawal. NABL 216
‘Procedure for dealing with adverse decisions’ gives the details.

National Accreditation Board for Testing and Calibration Laboratories 24/41

12. Surveillance and Re-assessment

NABL applies an assessment programme comprising of annual desktop surveillance during

each accreditation cycle of 2 years. At the end of the accreditation cycle, an on-site re-
assessment is conducted covering representative scope of accreditation. The NABL
accreditation certificate is valid for a period of 2 years. NABL conducts annual Desktop
Surveillance which is aimed at evaluating continued compliance with ISO/IEC 17025:2005 or
ISO/IEC 17025:2017 or ISO 15189: 2012 or ISO/IEC 17043:2010 or ISO 17034:2016
whichever is applicable and relevant NABL specific criteria (wherever applicable) and
Policies. The types of assessments are given below:

Desktop Surveillance

The desktop surveillance consists of calling of records from the CAB to ascertain that the
CAB continues to maintain the requirements of ISO/IEC 17025:2005 or ISO/IEC 17025:2017
or ISO 15189: 2012 or ISO/IEC 17043:2010 or ISO 17034:2016 whichever are applicable
and relevant NABL specific criteria (wherever applicable). NABL conducts annual desktop
surveillance during each accreditation cycle of 2 years.

Reassessment

The accredited CAB is subjected to re-assessment every 2 years. The CAB has to apply 6
months before the expiry of accreditation to allow NABL to organize assessment of the CAB,
so that the continuity of the accreditation status is maintained.

The renewal application is submitted in the prescribed form (NABL 151/ NABL 152/ NABL
153/ NABL180/ NABL190) in three copies along with two copies of Quality Manual of the
CAB which describes the latest management system in accordance with ISO/IEC
17025:2017 or ISO 15189: 2012 or ISO/IEC 17043:2010, ISO 17034:2016 whichever is
applicable.

The application is to be accompanied by the prescribed renewal fee, as detailed in the

application form. The CAB may request extension to the scope of accreditation, which should
explicitly be mentioned in the application form.

National Accreditation Board for Testing and Calibration Laboratories 25/41

13. Appeals and Complaints

Appeals

NABL is open to appeals from the CABs against its decisions. The decisions against which
appeals are entertained relate to denial of accreditation, reduction of scope of accreditation
or abeyance/ suspension/ forced withdrawal of accreditation. The details are provided in
NABL 134 ‘Procedure for Dealing with Appeals against Adverse Decisions Taken by NABL’.

Complaints

NABL is open to receiving complaints for any of the activities performed by its officials,
assessors, accreditation committee members and the accredited CABs. The details are
provided in NABL 132 ‘Procedure for Dealing with Complaints’.

National Accreditation Board for Testing and Calibration Laboratories 26/41

14. Rights and Obligations of CABs

Rights of CABs

 CABs are entitled to receive information related to CAB accreditation. They can access
NABL’s website www.nabl-india.org which gives information necessary for NABL
accreditation. 

 NABL is obliged to make available information on CAB’s scope of accreditation, validity
dates for its accreditation certificate(s) and contact details to users of the CABs. This
information is provided at NABL web -site. 

 The CABs are free to approach any accredited CAB for traceability of measurements
provided they fulfill the conditions laid down in NABL 142 ‘NABL Policy on Calibration
and Traceability of Measurements’.

 CAB has the right to object to appointment of specific member(s) of assessment team
by giving valid reasons. 

 NABL accredited CAB has the right to use ‘NABL Symbol’ on the test/ calibration
reports issued by it as long as the test/ calibration is included in its scope of
accreditation. Detailed requirements governing use of ‘NABL Symbol’ and claim of
accreditation have been stated in NABL 133. 

 NABL is open to receiving complaints for any of the activities performed by its officials,
assessors, accreditation committee members and the accredited CABs. 


 NABL is open to appeals from the CABs against its decisions. The cases may involve
refusal of accreditation, scope reduction, abeyance, suspension or forced withdrawal. 

National Accreditation Board for Testing and Calibration Laboratories 27/41

 Obligations of the CABs

 An accredited CAB is obliged to fulfill requirements of relevant standard and NABL

Specific Criteria (wherever applicable) and NABL 131 ‘Terms and conditions for
maintaining NABL accreditation’, at all times. 

 The CAB is obliged to disclose name of the consultant; if applicable, at the time of
applying for accreditation. 

 The CAB is expected to provide access to all premises where key activities of CAB are
performed and afford access to all relevant information, documents and records
necessary to assess CAB’s compliance to the relevant criteria, standards and NABL
131. 

 The CAB is expected to facilitate work of the assessment team by providing necessary
amenities including arrangement of appropriate test samples/ devices for calibration
and staff to demonstrate tests/ calibrations/ PTP and RMP activities. 

 An accredited CAB can claim accreditation only with respect to the scope for which it
has been granted accreditation as detailed in NABL 133, and not use accreditation in a
manner to bring disrepute to NABL. 

 The CAB is required to notify NABL of any change that may affect the ability of the
CAB to fulfill requirements of accreditation, within 15 days. Notifiable changes include
(but are not restricted to): change in legal status, change in ownership, changes in
organization, change in top management, change in key personnel and authorized
signatories, major change in policies, change in locations etc. 

 The CAB is required to pay necessary fees as determined by NABL from time to time. 

National Accreditation Board for Testing and Calibration Laboratories 28/41

 15. Rights and Duties of NABL

Rights of NABL

 NABL requires that all CABs will conform to ISO/IEC 17025:2017 or ISO 15189: 2012
or ISO/IEC 17043:2010 or ISO 17034:2016 whichever is applicable and relevant NABL
specific criteria (wherever applicable) to seek and maintain accreditation and adapt to
the changes in the requirements of accreditation. 

 NABL requires that all accredited CABs will sign NABL 131 ‘Terms and conditions for
obtaining and maintaining NABL accreditation’ and abide by it. 

 NABL has the right to: 

- effect changes in standards on which CAB accreditation is based in accordance
with international norms

- decide on policies related to accreditation in consultation with stakeholders

- appoint assessment teams in consultation with CAB and the assessors

- decide on implementation schedules in consultation with the CABs

- take action against CAB giving valid reasons for the same

- take adverse decisions giving reasons for the same

National Accreditation Board for Testing and Calibration Laboratories 29/41

Duties of NABL

 NABL is obliged to make available information on CABs’ scope of accreditation, validity

dates for its certificate(s) and contact details to users of the CABs. This information is
provided at NABL web -site. 

 NABL is obliged to provide information on Mutual Recognition Arrangement (MRA) with
APAC and ILAC partners and other International arrangements. The information is
provided on NABL web -site and more information can also be provided on request. 

 NABL provides the CAB with information about suitable ways to obtain traceability of
measurement relevant to the scope for which accreditation is granted. The information
is provided in NABL 142 ‘Policy on Calibration and Traceability of Measurement’.
Further, the details of calibration laboratories accredited by NABL can be obtained from
Laboratory search option provided on NABL website.

 NABL communicates changes to the requirements of accreditation such as ISO/ IEC

17025 or ISO 15189 or ISO/IEC 17043 or ISO 17034:2016, ILAC & APAC documents,
NABL specific criteria (wherever applicable) documents or any other requirements
through NABL website. NABL gives sufficient notice to the laboratories to enable them
to implement the changes. 

 NABL provides adequate mechanism to resolve complaints received for any of the
activities performed by its officials, assessors, accreditation committee members and
the accredited CABs.


 NABL provides adequate mechanism to address the appeals received from the CABs
against its decisions.

National Accreditation Board for Testing and Calibration Laboratories 30/41

16. NABL Finance and NABL Fee Structure

NABL Finance

NABL derives its funds from the revenue generated through accreditation activities.

NABL Fee Structure

A uniform fee structure is maintained for all CABs and the charges are maintained at a
reasonable level so that CABs are not denied participation in the accreditation process because
of unreasonable financial conditions. The information about the fee structure for various field(s)/
discipline(s) is given below:
FY 2018-19 FY 2019-20

Application Testing Laboratories: Rs. 11,000 Rs. 11,000

Fee For 01 product group/ discipline (eg. Metals & alloys,
Food & agricultural products, Drugs & pharmaceuticals,
(non-refundable, to Textiles etc.)
be paid along with
the application) Forensic Laboratories Rs. 44,000 Rs. 44,000
Laboratories under Integrated Assessment: Rs. 25,000 Rs. 25,000
(For 01 product group/ discipline)

Medical Laboratories (covering all fields) &

Associated Sample Collection
Centre/Facility (SCF)
Small Laboratories (below 100 patients/ day/location+) Rs. 18,700 + Rs. 18,700 +
Rs. 200 per Rs. 200 per
SCF SCF
Medium Laboratories (101-400 patients/ day/location+) Rs. 44,000 + Rs. 44,000 +
Rs. 200 per Rs. 200 per
SCF SCF
Large Laboratories (401-1000 patients/ day/location+) Rs. 1,10,000 + Rs. 1,10,000
Rs. 200 per + Rs. 200 per
SCF SCF
Very Large Laboratories (above 1000 patients/ Rs. 2,20,000 + Rs. 2,20,000
day/location+) Rs. 200 per + Rs. 200 per
SCF SCF
+ Multilocation laboratory - A Medical laboratory with more than one location in the same district,
with same legal identity.

Note: Application fee for Multi-location Medical laboratory shall be the fee of one location based
on number of patients received per day at that location plus the fee of second location based on
number of patients received per day and so on………..
Medical Imaging- Conformity Assessment
Bodies (MI-CAB): N/A Rs. 11,000
For 01 group/ modality (e.g. Computed Tomography,
Ultrasound and Colour Doppler)

Calibration Laboratories:
Mechanical – For 01 group (eg. Dimension, force etc) Rs. 11,000 Rs. 11,000
Electro-Technical (all parameters) Rs. 33,000 Rs. 33,000
Thermal (all parameters) Rs. 22,000 Rs. 22,000
Fluid Flow (all parameters) Rs. 22,000 Rs. 22,000
Optical (all parameters) Rs. 22,000 Rs. 22,000
Radiological (all parameters) Rs. 22,000 Rs. 22,000
Medical Devices (Upto 10 equipments) Rs. 50,000 Rs. 50,000

National Accreditation Board for Testing and Calibration Laboratories 31/41

 Proficiency Testing Providers:
For one scheme per field Rs. 25,000 Rs. 25,000
Additional Proficiency Test Item (matrix / group Rs.10,000 Rs.10,000
/ field)

Reference Material Producers:

Per Category – upto 2 sub-categories Rs. 25,000 Rs. 25,000
For each additional sub category Rs. 5,000 Rs. 5,000

Enhancement Testing Laboratories

of Scope (apart Any extension in the existing accredited scope Rs.5,500 per Rs.5,500 per
per discipline of testing group group
from the scheduled
re-assessment) For each additional product group in each Rs.11,000 Rs.11,000
discipline of testing
Any extension in the existing accredited product Rs. 25,000 Rs. 25,000
group per discipline under Integrated
Assessment
Medical Laboratories & Associated Sample
Collection Centre/Facility (SCF)
Any extension in the existing accredited scope Rs. 5,500 Rs. 5,500
Any addition in Sample Collection Centre/Facility Rs. 200 per Rs. 200 per
(SCF) SCF SCF
Medical Imaging Conformity Assessment
Body (MI-CAB)
Any extension in the existing accredited scope NA Rs. 5,500
of MI-CAB
Any extension of new group/ modality in the NA Rs. 11,000
existing accredited scope of MI-CAB
Forensic Laboratories
Any extension in the existing accredited scope Rs. 5,500 Rs. 5,500

Calibration Laboratories:
Mechanical – Any extension in the existing Rs.5,500 Rs.5,500
accredited scope per group per discipline
For each additional product group per discipline Rs.11,000 Rs.11,000
For extension in Electro-Technical, Thermal, Rs. 5,500 Rs. 5,500
Fluid Flow, Optical, Radiological disciplines
Medical Devices (Upto two equipments) Rs. 5,500 Rs. 5,500

Proficiency Testing Providers:

Additional Proficiency Test Item (matrix / group Rs.10,000 Rs.10,000
/ field)

Reference Material Producers:

For each additional sub category Rs. 5,000 Rs. 5,000

Change in Any addition of authorized signatory(s) apart from Rs. 5,500 / Rs. 5,500 /
the scheduled assessment request request
Authorized
signatory

National Accreditation Board for Testing and Calibration Laboratories 32/41

 Change of Testing, Calibration and Medical Laboratories-
Certificate Any change in the name and or premises of the Rs. 5,500 Rs. 5,500
laboratory leading to issue of new accreditation
certificate with scope
Any change in the name and or premises of the
Medical Imaging- Conformity Assessment Body NA Rs. 5,500
(MI-CAB) leading to issue of new accreditation
certificate with scope
RMP & PTP-
Any change in the name and or premises of the Rs. 3,000 Rs. 3,000
laboratory leading to issue of new accreditation
certificate with scope

Annual Testing laboratories (# including Integrated Rs. 24,000 Rs. 24,000

Accreditation Assessment) except Forensic laboratories
(per discipline):
Fee (per year from Forensic laboratories Rs. 48,000 Rs. 48,000
the date of
accreditation)
Calibration laboratories (per discipline) Rs. 24,000 Rs. 24,000
except Electro-technical calibration laboratories
Note-
Electro-technical laboratories Rs. 36,000 Rs. 36,000
Annual Accreditation
fee is payable in RMP & PTP Rs. 27,500 Rs. 27,500
advance and is non-
refundable and non-
adjustable. Medical Laboratories (covering all disciplines)
In case of co- & Sample Collection Centre/Facility (SCF)
terminus of Small Laboratories (upto 100 patients/ day/location+) Rs. 20,000 + Rs. 20,000 +
accreditation validity, Rs. 1,000 per Rs. 1,000 per
the fee will be
charged on pro-rata SCF SCF
basis Medium Laboratories (101-400 patients/ day/location+) Rs. 48,000 + Rs. 48,000 +
Rs. 1,000 per Rs. 1,000 per
SCF SCF
Large Laboratories (401 -1000* patients/ day/location+) Rs. 1,20,000 + Rs. 1,20,000
Rs. 1,000 per + Rs. 1,000
SCF per SCF
Very Large Laboratories (above 1000 patients/ Rs. 2,40,000 + Rs. 2,40,000
day/location+) Rs. 1,000 per + Rs. 1,000
SCF per SCF
Medical Imaging Conformity Assessment NA Rs. 24,000
Body (MI-CAB)
+ Multilocation laboratory – A Medical laboratory with more than one location in the same
district, with same legal identity.

Note: In case of Medical laboratory having Multi-locations, Annual Accreditation fee shall be
charged based on the location with maximum number of patients per day.

Overhead For each assessment including Desktop Rs. 11,000/- Rs. 11,000/-
Charges surveillance, irrespective of number of
disciplines

Assessment
Comprising of -Travel, Boarding, Lodging
Charges - Honorarium for NABL Assessors
(payable after the - Overhead Charges
completion of
assessment visit to For Sample Collection Centre / Facility (SCF) charges on Rs. 5,000 per
the CAB) lump-sum basis including Honorarium, travel and overhead SCF
expenses

National Accreditation Board for Testing and Calibration Laboratories 33/41

 Travel, The CAB will make the travel arrangements for assessors as per the
Boarding and following entitlements. Any travel or boarding and lodging beyond the
following entitlement shall be agreed upon in advance by the CAB under the
Lodging
intimation to NABL.
expenditure
A. Travel
 If the journey is more than 300 Km, travel to be made by Air in economy
class (Apex fare).
 If the journey is upto 300 Km, travel to be made by train in 2nd AC Class /
AC Chair Class or by AC Bus.
 If outstation journey is made by own car, the reimbursement will be
restricted to 2nd AC class fare by train.
 Travel within the city by taxi will be reimbursed on production of receipts /
bills. In absence of taxi bills or travel by own car within the city, claim will be
reimbursed @ Rs.15 per km.
 Any other relevant expenses during the travel will be reimbursed only on
production of receipts / bills.

 Boarding and Lodging
 A single occupancy AC accommodation to be provided for each Assessor
and Observer in a reasonably good hotel / guesthouse and arrangement for
local transportation from temporary residence to the CAB site and airport /
railway station / bus stand to be made.
 The CAB shall pay for meals of Assessor/ Observer during the stay, within
the reasonable limitations.

Note: The travel, boarding & lodging for NABL Officials joining assessment
as Observer, shall be borne by NABL.

Honorarium Document review by Lead Assessor Rs. 2,000

for NABL Pre-Assessment, Assessment, Verification, Special Visit
Assessors - by Lead Assessor Rs. 4,500 per
day
- by Technical Assessor/ Expert Rs. 4,000 per
day

Note: In addition to the above-mentioned fee, GST @ 18.0 % is to be paid along with said charges / fees.

# Additionally, ‘Testing laboratory under Integrated Assessment’ shall also directly pay the applicable annual
approval fee as prescribed by respective Regulatory Body.

National Accreditation Board for Testing and Calibration Laboratories 34/41

Fee Structure for Quality Assurance Scheme-Basic Composite Medical
Laboratories (Entry Level)

Components Fee / Charges

Application Fee Rs. 1,000/-

(non-refundable, to be paid along with the application)

Annual Membership Fee (for cycle of 02 years) Rs. 2000/-

Assessment Charges Rs. 10,000/-

(payable after the completion of assessment visit to the CAB)

Note: In addition to the above-mentioned fee, GST @ 18.0 % is to be paid along with said charges / fees.

National Accreditation Board for Testing and Calibration Laboratories 35/41

Fee Structure for Accreditation of Overseas Conformity Assessment
Bodies outside India
FEE STRUCTURE FOR SAARC COUNTRIES
(Effective from 15.01.2018)
(A) For Accreditation -
Application Fee 400 USD/ discipline (e.g. Mechanical
testing, Medical testing, Electro–technical
calibration etc.)
Document Review 200 USD
Assessment Charges 100 USD/ Man day
(B) To maintain Accreditation -
Accreditation Fee 350 USD/ Annum/ discipline
Desktop Surveillance Fee 200 USD
(C) Changes, if any -
Change in Authorized signatory 100 USD/ Request
Enhancement of Scope (apart from the 200 USD/ Product group
scheduled re-assessment)
Change of Certificate 100 USD
(Any change in the name and or premises of
the laboratory leading to issue of new
accreditation certificate with scope)

FEE STRUCTURE FOR OVERSEAS CABs OTHER THAN SAARC COUNTRIES

(Effective from 15.01.2018)
(A) For Accreditation -
Application Fee 1000 USD / discipline (e.g. Mechanical
testing, Medical testing, Electro –
technical calibration etc.)
Document Review 500 USD
Assessment Charges 600 USD/ Man day
(B) To maintain Accreditation -
Accreditation Fee 1000 USD/ Annum/Field
©(C) Changes, if any -
Change in Authorized signatory 250 USD/ Request
Enhancement of Scope (apart from the 300 USD/ Product group
scheduled re-assessment)
Change of Certificate 200 USD
(Any change in the name and or premises of
the laboratory leading to issue of new
accreditation certificate with scope)

Note: 1) Overseas CABs to contact NABL for making the payments

2) All charges (whether in India or abroad) incurred during wire transfer in foreign currency, shall be borne
by the CAB

National Accreditation Board for Testing and Calibration Laboratories 36/41

 Entitlement of Assessment–Team -

The laboratory/ PTP/ RMP shall make arrangements for Travel, boarding & lodging for the
assessment team. A single occupancy accommodation may be provided for each Assessor/
Observer in a good hotel and arrangement for local transportation from temporary residence
to the laboratory/ PTP / RMP site & airport.

The Laboratory / PTP/ RMP shall assist in VISA and arrange other logistics like travel
insurance and accommodation.

National Accreditation Board for Testing and Calibration Laboratories 37/41

17. Modes of Payment

S. Options Remarks
No.
1 Cheque / Demand Draft in favour of  No account number or branch to be
‘Quality Council of India’ payable at mentioned on Cheque / DD. Payee should
Gurugram / Gurgaon be only ‘Quality Council of India’;
 Cheque / DD to be sent to NABL Office at
the following address:
Plot no. 45, Sector 44,
Gurugram, Haryana – 122003.

2 Payment gateway for making online Gateway may be accessed from the home
payments page of NABL website.
 Existing CABs may obtain the Login
(Preferred and easiest method as credentials from NABL;
payment is easily traceable and  New CABs may pay directly through
reconcilable in an accurate and timely gateway without any login.
manner)

3 NEFT to following account :  Virtual Account no. will be unique for each
CAB and to be obtained from NABL;
Quality Council of India  Use only this virtual account no. for
HDFC Bank making all payments related to that CAB;
Kanjurmarg Branch, Mumbai  Use correct virtual account number to
IFSC Code – HDFC0004989 avoid the payment being accounted for
against wrong CAB Id;
Virtual A/c No. – Unique for each CAB,  Do not use any other account of ‘Quality
to be provided by NABL. Council of India’ for NEFT.

National Accreditation Board for Testing and Calibration Laboratories 38/41

18. NABL Publications

Sl. Name of Document Doc. No.

1. General Information Brochure NABL 100

2. Procedure for Recognition of Sample Collection Centre/ Facility declared by Medical NABL 111
Laboratories (CABs)
3. Specific Criteria for Accreditation of Medical Laboratories NABL 112

4. Guidance for Classification of Product Groups in Testing & Calibration Field NABL 120

5. Specific Criteria for Calibration of Medical Devices NABL 126

6. Procedure for Integrated Assessment & Additional Requirements of Regulatory Body NABL 127
(ies) for Testing Laboratories
7. Procedure for Quality Assurance Scheme for Basic Composite Medical Laboratories NABL 128
(Entry Level)
8. Specific Criteria for Accreditation of Calibration Laboratories NABL 129
(Mechanical, Fluid flow, Radiological, Electro-Technical & Thermal Calibration)
9. Specific Criteria for Site Testing and Site Calibration Laboratories NABL 130
10. Terms & Conditions for Obtaining and Maintaining NABL Accreditation NABL 131

11. Procedure for Dealing with Complaints NABL 132

12. NABL Policy for Use of NABL Symbol / Claim of Accreditation by Accredited NABL 133
Conformity Assessment Bodies (Laboratories / PTP / RMP) & NABL Accredited CAB
Combined ILAC MRA Mark
13. Procedure for Dealing with Appeals against Adverse Decisions taken by NABL NABL 134
14. Specific Criteria for Accreditation of Medical Imaging- Conformity Assessment Bodies NABL 135
15. Guidelines for Estimation and Expression of Uncertainty in Measurement NABL 141

16. Policy on Calibration and Traceability of Measurements NABL 142

17. Policy on Calibration and Measurement Capability (CMC) and Uncertainty in NABL 143
Calibration
18. Application Form for Testing Laboratories NABL 151

19. Application Form for Calibration Laboratories NABL 152

20. Application Form for Medical Testing Laboratories NABL 153

21. Application Form for Integrated Assessment of Testing Laboratories NABL 154

22. Application Form and Checklist for Quality Assurance Scheme for Basic Composite NABL 155
Medical Laboratories (Entry Level)
23. Application Form for Medical Imaging- Conformity Assessment Bodies (MI-CAB) NABL 156

24. Guide for Preparing a Quality Manual NABL 160

25. Guide for Internal Audit and Management Review for Conformity Assessment Bodies NABL 161
(Laboratories / PTP / RMP)
26. Policy for Participation in Proficiency Testing Activities NABL 163

27. Guidelines for Inter-Laboratory Comparison for Calibration Laboratories where formal NABL 164
PT programs are not available
28. NABL’s Policies for Accreditation ( as per ISO/IEC 17025:2017) NABL 165

National Accreditation Board for Testing and Calibration Laboratories 39/41

 29. Sample Calculations for Uncertainty of Measurement in Electrical Testing NABL 174

30. Application Form for Proficiency Testing Providers (PTP) NABL 180

31. Specific criteria for PT Provider Accreditation NABL 181

32. Pre-assessment guidelines and forms (based on ISO/IEC 17043:2010) NABL 182

33. Assessment forms and checklist (based on ISO/IEC 17043: 2010) NABL183

34. Application Form for Reference Material Producers (RMP) NABL190

35. Specific Criteria for Reference Material Producer Accreditation NABL191

36. Pre-Assessment Guidelines & Forms (based on ISO Guide 34:2009) NABL192
37. Assessment Forms And Checklist (based On ISO Guide 34:2009) NABL 193

38. Assessment Forms And Checklist (based On ISO 17034:2016) NABL 194
39. Procedure for dealing with Changes in Accredited Conformity Assessment Body’s NABL 201
Operations
40. Pre-Assessment Guidelines and Forms (based on ISO 15189:2012) NABL 208

41. Pre-Assessment Guidelines and Forms (based on ISO/IEC 17025) NABL 209

42. Assessor Guide NABL 210

43. Operational Manual for online Assessment (For Assessors) NABL 213
44. Assessment Forms & Checklists (based on ISO/ IEC 17025:2005) NABL 215

45. Procedures for Dealing with Adverse Decisions NABL 216

46. Assessment Forms & Checklists (based on ISO 15189:2012 ) NABL 217
47. Desktop Surveillance NABL 218

48. Assessment Forms and Checklist (Based on ISO/IEC 17025:2017) NABL 219

49. Document Review Checklist ( as per ISO/IEC 17025:2017) NABL 220

50. Assessment Forms and Checklist (Medical Imaging- Conformity Assessment Bodies) NABL 222

51. Bio-data of Assessors NABL 221

52. Contract between NABL and Assessors NABL 230

53. Directory of Accredited Testing Laboratories NABL 400

54. Directory of Accredited Calibration Laboratories NABL 500

55. Directory of Accredited Medical Testing Laboratories NABL 600

56. Directory of Accredited PTP NABL 700

57. Directory of Accredited RMP NABL 800

Note: All NABL documents can be downloaded free of cost from NABL website: www.nabl -india.org.

National Accreditation Board for Testing and Calibration Laboratories 40/41

19. Contact Details

Secretariat: National Accreditation Board for Testing and

Calibration Laboratories (NABL)
NABL House,
Plot No. 45, Sector 44,
Gurugram - 122002,
Haryana, India
Tel. no.: +91-124-4679700 (30 lines)
Fax: +91-124-4679799

Website: www.nabl-india.org
Email: [email protected]

National Accreditation Board for Testing and Calibration Laboratories 41/41

National Accreditation Board for Testing and Calibration Laboratories (NABL)
NABL House,
Plot No. 45, Sector 44,
Gurgaon - 122002, Haryana, India
Tel. no.: +91-124-4679700 (30 lines)
Fax: +91-124-4679799
E-mail: [email protected]
Website: www.nabl-india.org