WHO WE ARE:
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
Global Director, ARQon Asia Regulatory & Quality Consultancy
Founder of ARPA (Asia Regulatory Professional Association)
Varian Medical Systems.
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.
Principal Investigator & Head of Translational Core
Regulatory Manager, Qritive Pte. Ltd.
Quality and Regulatory Affairs Lead, Medtronic
Healthcare & Life Sciences Director, KPMG
Consortium Manager, Singapore Health Technologies Consortium
Regulatory Affairs & Quality Assurance Manager, South East Asia, ConvaTec
Chief Operating Officer, Endomaster
Chief Technology Officer, Osteopore International Pte Ltd
Regional QA Manager, Teleflex