This training course describes the regulatory framework and the general pathway for medical device registration in Singapore.
The course begins with an overview of the regulatory pathway in Singapore with an emphasis on the current regulations implemented by the authority.
We work through the basics of each step of the registration process and explain how medical device dossiers are compiled to conform to Singaporean regulations and are submitted online for approval to the Health Sciences Authority. The execution of all work within the main workflow will be covered with details of tasks, assessments, timelines and costs.
The course will provide you with a good insight into the Singaporean regulatory system and sound knowledge from beginning of registration through the other stages of product life cycle.
- Understanding the regulatory framework in Singapore.
- Understanding the general pathway for medical device registration in Singapore
Who Should Enroll:
Regulatory Affairs, Local Authorized Representative, Medical Device Manufacturers, Medical Device Distributors, Healthcare Professionals, Medical Device Practitioners, Investors in Medical Device Sector
Full Rebate from Us!
If you engage Andaman Medical within 1 year for regulatory services such as product registration and local representation in Singapore, the payment for this program will be offset against any future invoices.