Wednesday, 29 March 2017 12:00-1:30pm ET
Sponsored by:
While IDMP is delayed again, there is a global trend in regulations that demand greater sharing of SPOR data, so companies cannot sit back and wait. To prepare for IDMP, ICSR E2B(R3), the Falsified Medicines Directive, and more, companies are driving to better master their substance, product, organization and referential data.
This webcast outlines different data management strategies and the role for regulatory information management. IDMP experts from Deloitte and Veeva will draw from projects with multiple Top 50 pharmas to identify the foundational elements of good data and associated process implications.
Regulatory Affairs Professionals Society (RAPS)5635 Fishers Lane, Suite 400Rockville, Maryland 20852
raps@raps.org+1 301 770 2920
JoinMy RAPS DashboardLearn More
About UsTerms of UsePrivacy Policy