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Our team seeks to set up a quality, one-stop portal where content has been vetted by professionals with years of experience on their belt. Only after meeting the high standards set by the expert panel does the content make it onto our platform. This will establish a quality brand which will set us apart from other training providers which will in turn, attract more content creators and students to join us.

“Affordable, quality training.”


        “Mountain of content, where to begin my training?”


Currently, there are many trainings/webinars/workshops both online and offline to provide training on medical device product life cycle knowledge. However, a common and major pain point heard from both individuals and organizations is that there is no reliable one-stop training portal. With the amount of trainings available, it is tedious for any one person to sieve through the different trainings.

E-IMDS Founders & Chair

May Ng 

E-IMDS Founder


Global Director, ARQon Asia Regulatory & Quality Consultancy




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Jack Wong

E-IMDS Founder

Founder of ARPA (Asia Regulatory Professional Association)



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James Chan 

E-IMDS Chair

 RAQA Manager,
Varian Medical Systems. 




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E-IMDS Quality Control Panel

Consists of group of experts with years of experience and deep knowledge of different sectors to assess and vet the training materials to maintain a high level of quality standard.

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Aishwarya Bandla

Principal Investigator & Head of Translational Core

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Encey Yao

Regulatory Manager, Qritive Pte. Ltd.




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Jonathan Loo

Quality and Regulatory Affairs Lead, Medtronic

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Chris Hardesty

Healthcare & Life Sciences Director, KPMG 



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Gordon Xiong

Consortium Manager, Singapore Health Technologies Consortium


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Kenneth Cheong

Regulatory Affairs & Quality Assurance Manager, South East Asia, ConvaTec


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Colin Tan

Chief Operating Officer, Endomaster



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Jing Lim

Chief Technology Officer, Osteopore International Pte Ltd

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Victor Tan

Regional QA Manager, Teleflex


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