New Electronic Reporting Requirements for Safety &
Pharmacovigilance: Are You Ready?
The safety and pharmacovigilance landscape is changing rapidly, and the new global standards for regulatory reporting – E2B(R3), eVAERS, eMDR, and IDMP – represent some of the most significant changes that the industry has seen in over a decade. Not surprisingly, implementing them requires planning and preparation from both safety and IT organizations.
Discover how these changes will affect your organization with this comprehensive brief which explores the following topics:
- Global vs. Regional Requirements
- Identification of Medicinal Products (IDMP)
- Solving the Challenges of Industry
Please also
download our recorded webcast which addresses this topic.
