This training course describes the regulatory framework and the general pathway for medical device registration in Indonesia.
The course begins with an overview of the regulatory pathway in Indonesia 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 Indonesian 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 Indonesian regulatory system and sound knowledge of registration.
- Understanding the regulatory framework in Indonesia
- Understanding the general pathway for medical device registration in Indonesia
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 Indonesia, the payment for this program will be offset against any future invoices.