Understanding the Medical Device Regulatory Pathway in Indonesia

Online Training Id: RP-I-001

USD 450.00

USD 450.00

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.

Learning Objectives: 

  • 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.

Femilia Aulina 

Femilia Aulina has been working in the Medical Device sector for more than 5 years as a Regulatory Affairs. She is a regulatory consultant in PT Andaman Medical Indonesia with a thorough specialized knowledge of regulations and product registration of medical devices in Indonesia.

She holds a degree in Bachelor of Science and Apothecary.

Online Training Highlights
Duration: 60 mins
Released On: 10/28/2019
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