Choosing the right COA can make or break your #clinicaltrials. Explore our latest key considerations for selecting optimal COA measures, from appropriateness to feasibility. Ensure your assessments truly capture what matters most: https://hubs.li/Q02S9djZ0
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What data does your IRT maintain? Is your randomization correct? Data quality is everything—which is why it is the #1 factor cited by clinical trial execs when choosing a new IRT vendor. Check out some more insights in our latest IRT webinar here: https://hubs.ly/Q02nhtFD0
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When it comes to transporting products around the world, it feels like there are endless factors to consider, forms to fill out, and rules to follow. This process is complex, but CNS Intertrans can effectively deal with it using 20 years of experience. Read more: https://lnkd.in/gg7aSyiQ #rorologistics
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Phlexglobal's #TMF Quality Review (also known as a "file review") offers an in-depth, line-by-line assessment of your Trial Master File (TMF), ensuring that you have a clear understanding of its quality, comprehensiveness, and punctuality. Don't miss out on this opportunity to gain valuable insights into your TMF's performance and compliance with Good Clinical Practice (GCP) standards and regulatory requirements for essential documents. Discover more about our TMF Quality Review service here:🔗 https://lnkd.in/g6WHism2 Remember, quality is one of the three key metrics of TMF Health. Make sure your TMF is up to par and compliant with industry standards by taking advantage of Phlexglobal's expertise. #TMFQualityReview #GCPCompliance
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Phlexglobal's #TMF Quality Review (also known as a "file review") offers an in-depth, line-by-line assessment of your Trial Master File (TMF), ensuring that you have a clear understanding of its quality, comprehensiveness, and punctuality. Don't miss out on this opportunity to gain valuable insights into your TMF's performance and compliance with Good Clinical Practice (GCP) standards and regulatory requirements for essential documents. Discover more about our TMF Quality Review service here:🔗 https://lnkd.in/g6WHism2 Remember, quality is one of the three key metrics of TMF Health. Make sure your TMF is up to par and compliant with industry standards by taking advantage of Phlexglobal's expertise. #TMFQualityReview #GCPCompliance
TMF Quality Review
phlexglobal.com
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Phlexglobal's #TMF Quality Review (also known as a "file review") offers an in-depth, line-by-line assessment of your Trial Master File (TMF), ensuring that you have a clear understanding of its quality, comprehensiveness, and punctuality. Don't miss out on this opportunity to gain valuable insights into your TMF's performance and compliance with Good Clinical Practice (GCP) standards and regulatory requirements for essential documents. Discover more about our TMF Quality Review service here:🔗 https://lnkd.in/g6WHism2 Remember, quality is one of the three key metrics of TMF Health. Make sure your TMF is up to par and compliant with industry standards by taking advantage of Phlexglobal's expertise. #TMFQualityReview #GCPCompliance
TMF Quality Review
phlexglobal.com
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A quality-first mindset is essential when evaluating potential eCOA and IRT vendors for your trial. Our new quality checklist equips you with key questions to ask as you evaluate new clinical trial tech to enable compliance and uphold the highest standards of data integrity and participant safety: https://hubs.ly/Q02GxPvZ0
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In a previous post I whinged about EMIS in terms of worsening reliability and performance - what I didnt say is I think the whole way we do EPRs needs to change. GP records have historically followed a SOAP system. Subjective, Objective, Assessment and Plan. I guess analogous to history examination differential diagnosis and management plan. However in reality they are a series of text entries which are a mess. The consultation screen if filled with rubbish. hundreds of admin messages, Accurx/Paco other messages, blood tests, attachments its sometimes difficult to work out where the patient was actually seen and while there are filters they are a pain and dont work well. so Requirement number 1 is - a better way of logging what is a consultation what is communication, what is admin, what is plan. The way we work has changed and practices are no longer in isolation. some staff work at multiple practices - some only need access to some not all patients. some things e.g. admin tasks like prescriptions/incoming workflows etc need to be able to be seamlessly done at scale with perhaps different practices engaged in sharing different tasks. so requirement 2 is dynamic scalability and loss of the thinking of a practice as the only unit. LEAN - TPS etc.. I can track a parcel from Vietnam I ordered to my door and know where it is every step of the way inc when the driver is 2 stops away so I can meet him at the gate yet I messaged the practice I'm registered with the other day about a form I need filling in and ive literally no idea where they are up to with it Our IT systems have no inbuilt process mapping - I cant track anything, I cant really count anything - managers find it difficult to manage as there are no easy metrics or performance figures - yes there are some bolt on products that add features but requirement 3 should be built in process mapping and tracking. clinically I kind of want the same. when a do a referral I never get told how long it has taken to type or send - has it been send - has it arrived. how many referrals do I have active our there how many of the pts ive referred have been seen what are they waiting for. I can probably pull some of this from e-rs but its not by default - if we want to move to an active case management approach I need a better understanding of what is happening to my pts - similarly a local renal conslutant writes amazing letters. they list all the pts problems - where he is up to with them - what hes tried what hes not - what's next - their last results etc... id love GP records to be like this - most as stated are encounter entries. some very brief some pages long - often poorly coded - often with no discernible plan no allocation or timescales - my computer friends tell me things like ?Jira do this well. Scrum masters know what is being done by whom and what is on time and what isnt. Given these type of project management software exist lets build that into the software.
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💡 Gain insights into the critical changes CMS applied to the Section 111 TPOC reporting process. Watch now on demand, Breaking down CMS’s Section 111 TPOC/WCMSA data collection process – what to know and how Verisk can help, and to learn how these TPOC/WCMSA changes will impact Section 111 reporting going forward. Watch here: https://ow.ly/ELuf30sBAPg #CMS #Section111 #WCMSA #TPOC #Medicare #Verisk
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💡 Gain insights into the critical changes CMS applied to the Section 111 TPOC reporting process. Watch now on demand, Breaking down CMS’s Section 111 TPOC/WCMSA data collection process – what to know and how Verisk can help, and to learn how these TPOC/WCMSA changes will impact Section 111 reporting going forward. Watch here: https://ow.ly/fMJ630sBMiP #CMS #Section111 #WCMSA #TPOC #Medicare #Verisk
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Chief Optimus at Adherence | ePRO digital AI/ML MMAS-4 MMAS-8 | Morisky Medication Adherence Scales
2moThe patient voice is filled with such useable data. Gaining actionable insights from asking the right questions, even if the trial is observational, emphasizes that in every aspect of healthcare, we are doing whats in the best interest of the patient. Interventional trials benefit the patient over time with follow up assessments that have a validated scoring method; with a benchmark and data points throughout, PI's can show meaningful improvements and results.