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
The Shoulds and Shouldn’ts of Electronic Systems and Data in Clinical Trials Intro With the word should being mentioned 569 times and constituting ~7% of the content (only outweighed by data – 618
Trial master file misfiles are a common occurrence, with as many as one in every 10 documents being misfiled. In some ways, misfiles are an even greater issue now with eTMF systems, where filing is
Introduction Well, first and foremost, welcome! Rob Jones has relinquished control and I’ve been given free rein to bring you the last blog in the series on TMF Management in Clinical Trials. Those
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