With the publication of the ISO IDMP EU Implementation Guide V2.0,
the actual implementation clock becomes a reality.
During this webinar, Remco discussed latest changes of the EU Implementation Guide, opened discussion points and new process as part of
the TOM. The webinar will provide you a solid basis and will answer any question that you might have with regards to the new
process and data requirements.
Reactions to the webinar:
“Fantastic overview of current state of IDMP and very useful and pragmatic – the best IDMP presentation I have seen.”
“Really good material and presentation, good knowledge for questions, thanks very much for allowing people to attend.”
“Great overview! Also helpful to see the implications being put in context of a pharma company.”
Hosted by Remco Munnik
Your host during this webinar is Remco Munnik, who is a member of the EU IG Focus Group chapter 2 and 3 and has been supporting EMA during the review and drafting of the EU Implementation Guide. Remco has over 20 years of experience in Regulatory Affairs, with a special focus on Global submission procedures, electronic submission (eCTD) and regulatory data management (xEVMPD, ISO IDMP and RIMS). He has worked at both pharmaceutical industry and consultancy. In addition, Remco has been directly involved in the development and roll-out of the EU Telematics environment and has in-depth knowledge of the systems. Remco is member of the EMA ISO IDMP Taskforce Product & Organisation group.