This training course describes the general pathway for regulatory framework and medical device registration in Philippines.
The course begins with an overview of the regulatory pathway in Philippines with an emphasis on the current system and the impending implementation of the new regulations by the authorities.
We work through the basics of each step of the licensing and product registration process and explain how medical device dossiers are compiled to conform to Philippine regulations and are submitted manually for approval to the Food and Drug Administration. 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 Philippine regulatory system and sound knowledge of registration.
- Understanding the regulatory framework in Philippines
- Understanding the general pathway for medical device registration in Philippines
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 Philippines, the payment for this program will be offset against any future invoices.