VAL 080 Validation Master Plan Sample PDF

Standard Operating Procedure
Title: Validation Master Plan
Department Validation/Technical Services Document no VAL-080

Prepared by: Date: Supersedes:
Checked by: Date: Date Issued:
Approved by: Date: Review Date:
1.0 DOCUMENT OWNER

Validation / Technical Services Manager
2.0 PURPOSE
The objective of this document is to outline the validation plan for a GMP Site and to ensure
that all the necessary structures are in place to facilitate validation.
The Validation Master Plan is designed to provide a planned and systematic framework
within which all validation activities will occur. This document will also ensure that the
manufacturing facilities comply with the local applicable GMP regulations and Site
requirements for validation.
3.0 SCOPE
This plan applies to all GMP Manufacturing facility. The site operation includes the
manufacturing, packaging, testing and distribution of Therapeutic and Consumer health care
pharmaceutical products.
This plan defines general validation requirements for all Direct Impact Systems and processes
that support manufacture, packaging, testing and distribution of human and veterinary
products.
Products manufacture and/or packed at the GMP facility may include non-sterile tablets,
capsules, ointments and suppositories or others therapeutic products such as hormone,
steroid, penicillin or antineoplastics.
3.1 Site Facilities

The design and operation of a GMP facility must embraces GMP considerations, as
defined by the applicable regulations, for the manufacture of finished pharmaceuticals,
applicable industry standards, corporate Quality Standards and Guidelines and
environmental and health and safety requirements.
Details of the identification and location of the site facilities and descriptive summaries of
the site’s major manufacturing facilities, including equipment, utilities, laboratories and
support facilities and services should be found in the Site Master Plan. The Site Master
Plan will also detail all drug products manufactured and general organisation charts with
names and titles for key positions.
4.0 RESPONSIBILITY \ BUSINESS RULES

The requirements for validation will be established through the following organisation
structure:
4.1 Site Quality Review Team
The Site Quality Review Team consists of the members from the management team.
This team may delegates the Validation functions to the Validation / Technical Services
Steering Committee.
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Equipment qualification provides documented evidence that the equipment
consistently and without detriment achieves and maintains parameters that could
directly or indirectly affect, product quality. Refer to SOP VAL-090 Equipment
Validation Guideline.
5.2.4 Computer Validation

Computer validation ensures that all computerised systems (including hardware and
software) that have a direct impact on product quality, operates as per the required
specifications and principles of GxP. Refer to SOP VAL-040 Computer System
Validation.
5.2.5 Utility Validation

Utility validation provides documented evidence that the utility systems that have a
direct impact on product quality, operate as per requirements and consistently and
without detriment achieves and maintains parameters that directly impacts product
quality. Refer to SOP VAL-095 Facility and Utility Validation Guideline.
5.2.6 Analytical Method Validation

Analytical method validation provides documented evidence that test methods are
effective, reproducible and repeatable. Refer to SOP LAB-135 Validation of
Analytical Test Procedures.
5.3 Validation Documentation Overview

All validation activities are conducted according to local validation procedures as defined in
Section 5.2.
Validation Documentation shall be organized and retained to allow for easy retrieval. Each
document shall be assigned a unique document code as per site procedure and shall be
retained in accordance with the site document retention procedures.
5.3.1 Validation Master Plan

This Validation Master Plan (VMP) documents the general approach to validation at
Site, Site. The requirements for specific validation activities will be defined in
guidelines and procedures.
5.3.2 Validation Project Plans

A Validation Project Plan or Project Commissioning and Qualification Plan shall be
used for the validation of complex projects. Simple projects may be managed by the use
of protocols or through the change control system together with supportive
documentation.
5.3.3 Validation Protocols

Protocols outline the scope of work and the specific activities and tests that are required
to complete the validation. They also contain the predetermined acceptance criteria for
the validation.
5.3.4 Validation Reports

A Final Validation Report is used to summarize and document a completed validation
study. The report serves as a certification of completion of validation.

Documentation (e.g. User Requirement Specifications, Vendor Operation and
Maintenance Manuals) must be available that describes the system including what the
system does, and how the system performs its functions. The documentation will be
used to perform the Impact Assessment and will serve as the basis for defining
validation acceptance criteria.
5.5.7 Validation Deviations

Deviations that occur during validation shall be documented and investigated in
accordance with site procedures.
5.5.8 Validation Acceptance and Approval

Each validation event will be reviewed and approved by authorised individuals as
detailed in the relevant guideline documents. Where applicable, a minimum of three
consecutive events conducted on a fixed process with the same predetermined
acceptance criteria will be required before the validation event is considered complete.
Specific acceptance criteria for validation projects will be detailed in validation
project plans and protocols.
5.5.9 Maintaining the Validated State

All processes and systems once validated will be maintained in a validated state
through the life cycle of the process / system. Following completion of validation
testing, all planned and unplanned changes with potential impact on validated systems
and/or processes shall be addressed by established change management procedures
(e.g. change control, deviation, investigations). These changes shall be assessed
against prior validation studies and an impact assessment performed as per site
procedure. Re-qualification and revalidation requirements are identified by the
following mechanisms:
 Change Control System
 Product Audits (includes review of Deviations and Cross Functional
Investigations)
 Periodic Review
Validated Systems and Processes are subject to Periodic Review. The results of the
periodic review shall be documented, reviewed, and approved by the VC. The review
may result in the need for additional studies. The periodic review frequency shall be
based on the results of risk assessment and regulatory requirements. Periodic reviews
shall be conducted within the time interval not to exceed five (5) years. Periodic
review of process validation may be combined with the Annual Product Records
Review. Where no significant changes have been made to the validated status, a
review with evidence that facilities, systems, equipment and processes meet the
prescribed requirements fulfils the need for revalidation.
6.0 DEFINITIONS / ACRONYMS
GMP Good Manufacturing Practice

PCQP Project Commissioning and Qualification Plan
VC Validation Committee
VMP Validation Master Plan
VPP Validation Project Plan


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Standard Operating Procedure

Title: Validation Master Plan

Department Validation/Technical Services Document no VAL-080

1.0 DOCUMENT OWNER

3.1 Site Facilities

4.0 RESPONSIBILITY \ BUSINESS RULES

5.2.4 Computer Validation

5.2.5 Utility Validation

5.2.6 Analytical Method Validation

5.3 Validation Documentation Overview

5.3.1 Validation Master Plan

5.3.2 Validation Project Plans

5.3.3 Validation Protocols

5.3.4 Validation Reports

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5.5.7 Validation Deviations

5.5.8 Validation Acceptance and Approval

5.5.9 Maintaining the Validated State

6.0 DEFINITIONS / ACRONYMS

GMP Good Manufacturing Practice

Copyright©www.gmpsop.com. All rights reserved

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