PrintSingapore passed the Health Products Act in February 2007. Under this Act manufacturers, dealers, importers and wholesalers of medical products will eventually require comprehensive government licensing in order to do business. The deadline for compliance is in 2009, so make sure you know the newest regulations before time runs out! 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.
See a sample page of our webcast presentation.
What you will learn:
- Overview of Singapore
- Economy
- Demographics
- Health Statistics
- Overview of Singapore Medical Device Market
- Profile of Singapore’s Health Sciences Authority (HSA)
- Organization
- Overview of Medical Device Regulatory Framework
- Product Registration Process
- Which Products Need to Be Registered
- Definitions
- Classification of Medical Devices
- Application Process
- Common Submission Dossier Template (CSDT)
- Actual Submission Fees and Timeframes
- How to expedite the registration process
- Advertisement and Promotion
- Reimbursement
- New Regulations
- Future Trends of Singapore’s Medical Device Market
This webcast is designed for medical deviceprofessionals in regulatory affairs, business development, international sales and marketing, and anyone who wants to be current on Singapore medical device issues.