AMERSHAM, United Kingdom and MALVERN, Pa., July 18, 2019 /PRNewswire-PRWeb/ -- Phlexglobal today announced an exciting series of complimentary seminars aimed at helping pharmaceutical companies reach meeting 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
United States Half-Day Seminars: THE TMF HEALTH ZONE: How to Get There, and How to Maintain TMF Health
Phlexglobal will host two half-day seminars focused on helping pharmaceutical companies understand the core principles and best practices required to achieve ongoing inspection-readiness for Trial Master Files - the "TMF Health Zone" - along with common challenges companies face in getting there. Presenters will provide key ways, with actual customer use cases, of how companies reach the TMF Health Zone and stay there.
Cambridge, Massachusetts: August 20
Morristown, New Jersey; August 21
Registration available at http://www.phlexglobal.com/SummerUS2019
About Phlexglobal
Phlexglobal provides the market-leading Trial Master File solution by leveraging dedicated and authoritative TMF technologies and expert services. The company offers a unique combination of sophisticated technology, clinical trial knowledge, regulatory understanding and document management skills to deliver a range of flexible, targeted solutions to meet business needs.
SOURCE Phlexglobal
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