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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.”


              Pain point:  “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 Quality Control Panel

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Aishwarya Bandla

Principal Investigator & Head of Translational Core

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Chris Hardesty

Healthcare & Life Sciences Director, KPMG 



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Colin Tan

Chief Operating Officer, Endomaster



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Encey Yao

Regulatory Manager, Qritive Pte. Ltd.


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James Chan 

 RAQA Manager,
Varian Medical Systems. 

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Gordon Xiong

Laboratory Manager / Research Scientist
National University of Singapore

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Jing Lim


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Jack Wong

Founder of ARPA (Asia Regulatory Professional Association)


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Jonathan Loo

Quality and Regulatory Affairs Lead, Medtronic

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Kenneth Cheong

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


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May Ng 

Global Director, ARQon Asia Regulatory & Quality Consultancy

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Victor Tan

Regional QA Manager, Teleflex

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