Course Description

Strategic Approach to Bringing Medical Devices to the Indonesian Market

Course Description:

This course provides a basic understanding of the current medical device regulatory environment in Indonesia and includes a step-by-step guide to constructing market access strategies for medical devices in Indonesia.

Watch the Course Trailer:



Learning Objectives:

Upon successfully completing this course, learners will be able to:

  • Perform the necessary steps in establishing a legal entity that ensures market access in Indonesia
  • Initiate successful relationships between manufacturers and local license-holders prior to and during market access
  • Demonstrate effective planning and appropriate measures to get medical devices to the Indonesian market

Who Should Enroll:

Regulatory Affairs Associate, Regulatory Affairs Manager, Quality Assurance Associate, Quality Assurance Manager, Quality Assurance Engineer, Manufacturing Engineer, Supply Manager, Purchasing Manager, Design Engineer, Validation Engineer, Electrical Safety Engineer, Internal Auditor, Lead auditor, Pre-Clinical Affairs Director, Clinical Project Manager, Export Manager, and R&D Engineer are all welcome to participate in this course.

Prerequisite Knowledge/Requirements:

There is no prerequisite knowledge required for this course; all areas of expertise are welcome.

Subject Matter Expert:
Fiametta Soenardi

50 min

Release date:

Related resources:

Case studies:

Basic Account: € 148.00
Premium Account: € 111.00

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