CBI’s 2nd Annual IDMP Update Forum is taking place on December 8-9, 2016 in Philadelphia (USA) and Asphalion’s Director of Regulatory Information, Remco Munnik, is participating as an expert speaker in the conference “ISO EMA SPOR
IDMP Task Force Address – Data Domain Development and Standards Progress “:
IDMP Task Force Address – Data Domain Development and Standards Progress “:
I. Gain Insight into EMA Perspective on IDMP Initiative
II. Examine Task Force Progress and Hear Real-Time Updates on Next Steps for Industry
III. Evaluate the Scope of the IDMP Initiative
IV. Assess EMA’s Proposed Timelines for IDMP Phased Approach to Implementation
V. Understand Potential Impact of Brexit on IDMP Timelines and Progress
Are you interested in market and/or manufacturing medicinal products in EU?
Then you must comply with the guidelines and requirements of IDMP (Identification of Medicinal Products)
Join the event to benchmark with peers and learn from industry champions on how to pro-actively address organizational and technical challenges for the global harmonization of product data and information.
