This event will enable you to effectively interpret complicated regulatory guidelines to fast track your drug approval process
Early Confirmed Speakers:
- Widyaretna Buenastuti, Public Affairs & Communications Director, Pfizer Indonesia
- May Ng, Regulatory And Quality Consultant,Founder, ARQon Pte Ltd
- Shibu Baburaj, Head, Regulatory Affairs, Sanofi-Aventi
- Dimas Adityo, Compliance Director/Head of Ethics & Business Integrity, Sanofi Indonesia
- Ranjodh Gill, Compilance Manager Quality Assurance, Parexel
- Rakesh Chaurasia, Head Drug Regulatory Affairs, PT Dexa Medica
Highlighted features at 2-day conference includes
- Regulatory submissions implementation in eCTD format
- The ASEAN Labelling Harmonisation Effort
- Registration and approval timeline – combination products and exemptions
- What’s new with clinical regulatory requirements in Asia Pacific?
- Global trends vs. specific region’s updates for pharmacovigilance
- Regulatory affairs support in providing advices to commercial team for inspection
- Global Guidelines for the Development of Biologics
Who Will Attend?
ACI’s summits attract a targeted group of senior level executives with a strict focus on end-users from the industry.
Directors/Heads/Managers of Regulatory Affairs, Quality Control, Quality Assurance, Patent/Intellectual Property Rights /Legal, Pharmacovigilance/Drug Safety
For Agenda/Event Brochure, Information & Registration, Contact:
Priyesh Waghmare
E: pwaghmare@acieu.net | T: +91 (0)20.6527.2803
Event Website: http://www.wplgroup.com/aci/event/pharma-regulatory-asia/
To request the Latest Agenda & more details on the Programme, Speakers and their Presentations by email, please click here>>
(Quote discount code: PRSf1MP15 to claim for 15% discount- For registration please contact Priyesh Waghmare)