Fundamentals of Medical Device Regulatory Affairs

Provided by NUS Academy of GxP Excellence

Course introduction



The objective of this course is to provide an overview to technical professionals, particularly those in Research & Development and Regulatory Affairs, on the general legal requirements to bring a medical device product to market – whether it is the creation of a new product, or import/export of a product to a new market.


This course will discuss medical devices in major international reference environments and select countries in Asia, medical device definitions and classifications. The course will discuss the major pre-marketing regulatory challenges and potential solutions in key Asian markets. Advanced products such as combination products are interpreted differently by different agencies, and there tends to be more disparity among Asian countries compared to more mature Western agencies. This course will discuss some of the challenges with such advanced products.

Course Outline

• Introduction to RA – what is the role of RA
• Introduction to major global reference regulations and harmonizations
   o US
   o Europe
   o Japan
   o Australia
   o Canada
   o GHTF
• Overview of regulatory environment in major Asian reference countries:
   o Singapore
   o China
   o Hong Kong
   o India
   o Future trends in regulatory development
• Pre-market requirements
   o Background
   o Classifications
   o GMP
   o Conformity assessment
• Advanced products:
  o Combination products
Learning Outcomes

Upon completion of this course the attendees will be able to:

1. Understand major global reference regulations and harmonization efforts for medical devices
2. Understand regulatory environment in key Asian markets for medical devices
3. Understand general pre-market requirements
4. Understand the legal logics behind the definition and regulation of advanced products

Fees & Funding

Please enquire below for course fees and financial grants:


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