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The new EMA TMF Guidance is now in effect. Are you ready?

The European Medicines Agency (EMA) guidance on Trial Master Files took effect on June 6, 2019 and promises to have far-reaching impacts on an organization’s TMF processes, technology, and best practices – as well as related departments and systems. 

Phlexglobal is offering this free guide by renowned TMF expert Eldin Rammell to help you better understand the impact this can have on your TMF management processes. 

Please complete this form to read the guide.

2019 EMA Guidlines
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