The UNICOM monthly interactive webinar sessions discuss IDMP further issues related to the identification of medicinalproducts in regulatory and clinical contexts. 

On Thursday, November 12th it addressed how substances/products have been selected for piloting, and how this is moving to support use of IDMP data across multiple domains of the medicinal product life cycle.

Introduction: Julie James (Bluewave Informatics, UNICOM WP 9 lead)

Other UNICOM Presenters:
Annet Rozema (Medicines Evaluation Board Agency – CBG, Netherlands)
Ursula Tschorn (IDMP1 Germany)
Robert Vander Stichele (University Gent, I~HD)
Moderator: Christian Hay (GS1)

Previous webinars are now available on UNICOM YouTube channel: 

• IDMP, Falsified Medicines Directive and Parallel Trade. 
• UNICOM – The PhPID (Unique identification for Pharmaceuticals products) 
• UNICOM – Gap Analysis about existing and new standards and profiles