Pharmacovigilance Asia 2010

Venue: Novotel Singapore Clarke Quay

Location: Singapore, Singapore

Event Date/Time: Oct 26, 2010 End Date/Time: Oct 27, 2010
Early Registration Date: Aug 27, 2010
Report as Spam


Pharmacovigilance and drug safety management in Asia are rapidly gaining attention in Asia with the shift of pharmaceutical activities from west to east. With an increasing number of clinical trials being held in the region and the rapidly growing markets for both pharmaceutical products and medical devices, the risk of ADEs/ADRs/SAEs has never been greater.

Every pharmaceutical/medical device company must address and manage drug safety risks and pharmacovigilance if they want to sustain the public’s confidence.

Are you taking the necessary steps to effectively manage pharmacovigilance and drug safety?

The Pharmacovigilance Asia 2010 held in Singapore on 26-27 October 2010 is a one of a kind event which will bring you PV regulatory updates from across Asia, and experts in pharmacovigilance and drug safety from pharmaceutical/biotech and CROs will discuss the most pressing issues faced in drug safety.

Key themes for Pharmacovigilance Asia 2010:

- Keeping up to date with changes to pharmacovigilence and drug safety regulations in Asia and worldwide
- Ensuring effective pharmacovigilance in clinical trials and in the post-marketing of drugs and devices
- The heterogeneity of safety requirements and pharmacovigilance systems in Asia and how Asia can move towards achieving a harmonized safety data exchange system
- What can be done to combat drug counterfeiting and to minimize the impact of substandard pharmaceuticals on drug safey and pharmacovigilance in Asia?
- Risk management and risk communication of ADE/ADR/SAE reporting


177A River Valley Road Singapore 179031