Global Pharmaceutical Regulatory Affairs Summit

Meet with the pharmaceutical regulatory community for improved knowledge, networking and experience exchange.

Regulatory Affairs in Emerging Markets: Get your burning questions answered in our; Russian GMP requirements interactive troubleshooting session; Q and A session on registration in Ukraine; Brazil and China QandA sessions; and Collaboration Zone round tables on Russia and CIS, Turkey and MENA, Latin America. and Asia-Pacific

Global eSubmissions: Join our; interactive round tables to share experiences with EU eCTD Module 1 Specification v3.0; Global Collaboration Zone to overcome challenges with global eCTD requirements; and our IDMP experience exchange as part of the IDMP Focus Day

Pharmaceutical Labelling: Join your peers in an interactive discussion forum examining strategies to improve communication between pharmacovigilance, labelling, regulatory affairs and risk management; overcome labelling challenges resulting from increasing serialisation and coding requirements by attending the in-depth serialisation workshop; and understand best practice for creating a CCDS suitable for global implementation with a dedicated CCDS workshop.

BOOK NOW TO SAVE
Book your tickets by Friday 23rd September 2016 to save £200

Price :
2 Day Pass - GBP 1499
Third Day Pass - GBP 600
Pre-Conference Evening Seminar - GBP 396