Global Pharmaceutical Regulatory Affairs Summit

Memo

Informa Connect Life Sciences are bringing the regulatory community together to discuss and address the industry's common concerns. Get involved with the discussion, to explore the latest insights and share thoughts on SPOR, eCTD, global regulatory submissions and serialisation from around the world. 4 key areas will be discussed; 1) Global eSubmissions, 2) Regulatory Information Management, 3) Regulatory Affairs in Global Markets, 4) Filing Variations. Discover the latest in the industry, so you can increase your submission success and have a clear understanding of the regulatory requirements when preparing for market access around the world. Network with 170+ regulatory professionals, join your peers from 100+ companies and learn more about the regulations in 14 countries. With leading speaker representatives from ANIVA, MEB, SPOR and IDMP Task Force across four tracks of leading content, can you afford to miss out? Sponsor: https://go.evvnt.com/577369-2?pid=5569 Speakers: Ching Li, Manager, Corporate Regulatory Affairs, Biotest Pharma GmbH, Frits Stulp, Project Manager EU-SRS, Medicines Evaluation Board, Patrícia Kott Tomazett, Health Regulation Specialist, General management of Drugs - GGMED, Brazilian Health Surveillance Agenda (ANVISA), Jörg Stüben, Head of Regulatory Information Management and Senior Expert, Boehringer Ingelheim On Monday September 07, 2020 at 9:25 am (ends Thursday September 10, 2020 at 3:30 pm)