To achieve and maintain ongoing TMF health and inspection readiness – the “TMF Health Zone” – requires experienced people trained on effective processes using the right technology.

Amersham, UK; Malvern, PA. — June 20, 2019 — Phlexglobal today announced an exciting series of complimentary seminars aimed at helping pharmaceutical companies meet regulatory guidelines and achieve optimum TMF Health.
United Kingdom Lunch and Learn Events:
What Rules & Regulations are Doing for TMF Health
Phlexglobal will host two Lunch and Learn events to present information about the new EMA Guideline on the Content, Management and Archiving of the TMF and how this may impact life sciences companies. There will be time for attendees to ask questions and discuss specific points in an informal setting as well as networking with industry colleagues. Lunch will be provided.
Cambridge, United Kingdom: 31 July
Details available at http://www.phlexglobal.com/CambridgeUK2019
Oxford, United Kingdom: 7 August
Details available at http://www.phlexglobal.com/OxfordUK2019
When my Trial Master File (TMF) career began, the TMF Reference Model did not exist. Every customer had a different way of organising the contents of their TMF, and it was rarely interpreted
Building the Right TMF Team for Inspection Readiness, Scalability and Growth As clinical trials become more complex, many Sponsors and CROs find themselves asking the same question: Do we need more
Why portfolio-level TMF oversight is becoming a necessity, not a luxury. The Problem With Thinking Study-by-Study Clinical trials do not happen in isolation. Sponsors and CROs are running multiple
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