Pan-Asia

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The Regulatory Affairs Professionals Society (RAPS) is the largest global organisation of and for those involved in regulation of healthcare and related products, including medical devices, pharmaceuticals, biologics and nutritional products.

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  • Online Learning
  • Graduate Certificate in Medical Devices
  • RAC
  • News/Intelligence
RAPS Online Learning Solutions

RAPS Online Learning Solutions

It’s Your Time. Learn Wisely.

  • Competency-based courses designed by regulatory experts
  • Rigorous and relevant for all career levels
  • Certificates offered in pharmaceuticals and medical devices
  • Regulatory Basics bundled courses for region-specific learning
  • Designed to be flexible and convenient
  • iPad/tablet accessible
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RAPS and NUS Team Up to Offer Graduate Certificate in Medical Devices

RAPS and NUS Team Up to Offer Graduate Certificate in Medical Devices

Singapore-based regulatory affairs professionals in the medical devices sector are invited to register for the Graduate Certificate in Medical Devices Regulatory Affairs (MDRA), jointly offered by RAPS and Asia’s top ranking university–the National University of Singapore (NUS).

Recognising that the profession demands unique knowledge and skills, as well as regulatory competency throughout the product lifecycle, the MDRA program builds the foundational knowledge, critical thinking and application skills required of regulatory professionals. The curriculum will be delivered through a combination of online training, interactive seminars, peer interaction and case-based learning.

Download the brochure and read what faculty say about the program.

Visit Program Website
Regulatory Affairs Certification (RAC)

Regulatory Affairs Certification (RAC)

An individual certification for our global industry

Join the ranks of the most successful regulatory professionals with your RAC. This accredited credential is the only globally recognised certification for the regulatory industry.

The RAC highlights your knowledge through a region-specific lens. Where is your expertise? 

  • RAC (Global): Knowledge and critical thinking skills related to the international practice of regulatory affairs, with special attention paid to global standards from ICH, GHTF (through IMDRF), WHO and ISO
  • RAC (EU): Knowledge of European Union regulations
  • RAC (US): Knowledge of US regulations
  • RAC (CAN): Knowledge of Canadian regulations
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Regulatory Focus/Regulatory Intelligence

Regulatory Focus/Regulatory Intelligence

Regulatory Focus is the leading source for quality, timely, regulatory news, information and analysis.

  • Easy to read daily regulatory intelligence through Regulatory Reconnaissance and a daily newsletter, RF Today—both of which are available free of charge
  • RAPS members receive access to in-depth articles written by regulatory professionals on topics of global and regional Interest
  • Information for regulatory professionals at all career levels and others interested in healthcare product regulation throughout product lifecycles
  • Read each month by more than 40,000 people around the globe
Read Now

Pan-Asia Office

Email: RAPSAsia@raps.org
Tel: +65 6496 5507
20 Bendemeer Road | #04-02 Cyberhub | SINGAPORE 339914

Introducing RAPS Pan-Asian Advisory Committee

RAPS is pleased to announce it has formed an advisory committee to guide its efforts in serving regulatory professionals well in Asia.  The Pan Asian Advisory Committee (PAAC) is part of RAPS’ global structure of regional advisory groups, alongside similar committees in China and Europe. The PAAC will provide strategic input on matters of regulatory capacity, regulatory practice, needs and opportunities from a Pan Asian perspective.   

RAPS PAN Asian Advisory Committee

Asst. Prof. Raymond Chua (Co-Chairman)
Group Director, Health Products Regulation Group
Health Sciences Authority, Singapore
Principal Director, HSA Academy

Mr. Torsten Fuehrer
Managing Director, South East Asia
Emergo Group

Mr. Jack E. Moore, Jr.
Director, Regulatory Affairs & Compliance, Greater Asia
BD

Dr. Raza Zaidi
Global Head, Regulatory Policy & Intelligence
Established Pharmaceuticals Division
Abbott Laboratories (Singapore) Pte Ltd

Dr. Wang Ming Che
Director, Division of Medical Devices
Center for Drug Evaluation, Taiwan

Dr. Khoo Teng Chuan (Co-Chairman)
Chief Medical Officer
Singapore Clinical Research Institute Pte Ltd

Ms. Jacqueline C. Monteiro
Director, Quality & Regulatory, Asia Pacific
Philips Healthcare
Philips Electronics (S) Pte Ltd

Dr. Meenakshi Rao
Director, Regulatory Strategist
Strategic Drug Development Asia
Quintiles East Asia Pte Ltd

Mr. Tan Kim Lee
Director, Quality
Flextronics Medical