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
How Senior TMF Study Owners bridge strategy, mentoring and operational delivery. What does it really mean to have an expert in your corner when it comes to your Trial Master File? For organisations
The critical role TMF Study Owners play in driving inspection readiness. The Cost of an Afterthought In the fast-paced environment of a clinical trial, where multiple activities unfold in parallel,
Why TMF Administrators are becoming essential to scalable TMF operations. The Invisible Engine Behind Every Healthy TMF Clinical trials are complex. Sponsors are under pressure. Timelines are tight.
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