DUBLIN--(BUSINESS WIRE)--Research and Markets (http://www.researchandmarkets.com/research/13782d/2011_singapore_med) has announced the addition of the "2011 Singapore Medical Device Updates" audioconference to their offering.
Singapore passed the Health Products Act in February 2007. This Act has been implemented in stages throughout the past few years. Under this Act, all medical devices Class A-D require product registration with the Singapore HSA. Also, manufacturers, dealers, importers and wholesalers of medical products require comprehensive government licensing in order to do business. Make sure you know the newest regulations in order to remain in compliance with Singapore law! Companies without the proper licensing will not be allowed to import, manufacture, or sell medical devices in Singapore. This 90-minute session will include a 60-minute presentation, followed by 30 minutes of Q&A.
Key Topics Covered:
What you will learn:
- Overview of Singapore
- Overview of Singapore Medical Device Market (Size, Growth Rate, Key Sectors)
- Profile of Singapore's Health Sciences Authority (HSA)
- Overview of Medical Device Regulatory Framework
- Product Registration Process
- New Regulations for Importers, Wholesalers, and Manufacturers of Medical Devices
- Post-Marketing Surveillance Responsibilities
- Advertisement and Promotion
- Reimbursement
- Future Regulatory Trends of Singapore's Medical Device Market
For more information visit http://www.researchandmarkets.com/research/13782d/2011_singapore_med