This training course describes the regulatory framework and the general pathway for medical device registration in Vietnam.
The course begins with an overview of the regulatory pathway in Vietnam with an emphasis on the current system and the implementation of new regulations by the authorities.
We work through the basics of each step of the registration process and explain how medical device dossiers are compiled to conform to Vietnamese regulations and are submitted online for approval to the Ministry of Health. The execution of all work within the main workflow will be covered with details of tasks, timelines and costs.
The course will provide you with a good insight into the Vietnamese regulatory system and sound knowledge of registration.
- Understanding the regulatory framework in Vietnam
- Understanding the general pathway for medical device registration in Vietnam
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 Vietnam, the payment for this program will be offset against any future invoices.