XEVMPD—The First Step to ISO-IDMP and Global Convergence

The European Commission has put in place a regulation (Article 57) mandating electronic submissions to medicinal products dictionaries for all medicinal products. In addition to creating immediate changes for the human medicines industry, this regulation is the flagship of global adoption of ISO IDMP (Identification of Medicinal Products) standards in support of ICH M5 by 2015–16.

This global convergence is creating a massive shift in regulatory. Organizations that proactively adopt practices and technology to comply with this change will benefit from the added ability of strategic decision making and dynamic resource planning. This webcast will equip regulatory professionals with the knowledge to prepare and meet the challenge of converging standards today and into the future.