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Trial Master file inspection ready. etmf inspection ready. outsourcing ready.

The most up-to-date insights from the TMF and eTMF world

Identify your weak spots through a mock inspection

Under the eye of a real authority, we’ll be hosting a mock inspection giving you an opportunity to have a run through of the areas you need to improve and work on to ensure you succeed in your next inspection.

Nothing better than a practice run..

Are you ready to make the jump to eTMF?

Case study from GSK, Biogen and Cancer Research, to make sure you’re ready for the transition:

  • Implementing eTMF and adopting the DIA TMF reference model
  • Moving to an eTMF system: Assessing the challenges and opportunities
  • Fully validated TMF vs hybrid: what are the pros and cons of both?
Tap into insights from the Regulatory Authorities and industry experts
  • Danish Medicines Agency
  • Roche
  • GSK
  • Cancer Research UK
  • Mylan 
  • Biogen 
  • Boehringer Ingelheim

and many more...