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)