Thursday, June 14th
15:00 PM – CEST / 09:00 AM EDT
Though hampered by a number of obstacles – the latest of which is the EMA’s relocation to Amsterdam – IDMP implementation in Europe continues to gather momentum.
With Organisations Management Services (OMS) as the initial part of EMA’s Substances, Products, Organisations & Referentials (SPOR) Master Data hub going live in 2017, industry has got its first flavour of how IDMP will impact regulatory processes in the future.
This webinar will provide an overview on how IDMP will affect our way of working in Regulatory Affairs and beyond, and what industry should do now to ensure they are prepared.
- The iterations and phases of SPOR implementation
- IDMP as a common language
- SPOR in the Framework of EU Telematics Strategy
- SPOR Impact on Industry – for example SME and Big Pharma
You may address your questions at: email@example.com
Director, Principal Consultant Regulatory Operations Industry/Agency Liaisons
A chemist by education, Karl-Heinz has spent the last 13 years in Regulatory Affairs, focussing on electronic submission, data management and systems implementation. He has been a member of EMA’s XEVMPD Implementation Working Group and the IDMP Implementation Task Force.