Trial Master File (TMF) quality control is a topic that always seems to be present on conference agendas and it invokes ...
Trial Master File (TMF) quality control is a topic that always seems to be present on conference agendas and it invokes ...
On April 16, 2020, the US Food & Drug Administration (US FDA) released an update1 to its March 2020 guidance on the ...
The next few months are going to be challenging in ways that we have never known. There are going to be different kinds ...
In early October, Phlexglobal was honored to welcome industry TMF professionals from over thirty pharmaceutical ...
Adapted from a March 2019 Phlexglobal webinar. For an in-depth look at the topic of migrating TMF data, view the ...
Adapted from an April 2019 Phlexglobal webinar presented by Eldin Rammell. For a more detailed discussion of the new ...
The adoption of Regulation (EU) 2017/745 on Medical Devices (MDR) and Regulation (EU) 2017/746 on In-Vitro Diagnostic ...
UK: +44 (0) 1494 720420
US: +1 (484) 324-7921
Poland: +48 81 45 46 132
Germany: +49 89 23514741
E-Mail: info@phlexglobal.com