ISO IDMP Implementation in Europe – how SPOR will change the Regulatory Environment

Duration: 1 hour & 10 minutes

Webinar Recording

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Why watch

Summary

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.

Key Learnings

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

speakers

A full day of inspirational speakers

Proud to bring inspirational speakers from across the globe.

Karl-Heinz Loebel

Director, Principal Consultant Regulatory Operations Industry/Agency Liaisons, PharmaLex

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.