Andrew See

Andrew See

Consultant
Medipro Consultancy and Services

Categories covered by Andrew

About this Speaker

Have been in the Medical Device Industries in Asia Pacific Region for the past 38 years worked with Baxter, Kendall, Otsuka Pharmaceticals, Ohmeda(BD), ClearLabs. Currently a QA Consultant working with Cardiac Lab. at National University Singapore in Class II and III Devices. I also Provide ISO13485:2016 QMS, IQA, Awareness, Implementation, Clause by Clause GDPMDS, MDR 2017/745, IVDR 2017/746, MDSAP, GMP, 21CFR Parts 820, Part 11, ISO10993 Medical Devices Biocompatibility and Medical Devices Design Development control, Process Validation and Different Methods of Sterilization (ETO, Gamma, Steam and Liquid Chemical) Training at TUV-SUD and B.S.I. Singapore. Worked as Production, QA, R&D Manager and General Manager before in the companies.

Well connected with Regulatory Bodies in the ASEAN and North Asia region to register clientele’s products in the region and liaises with them for all regulatory affairs issues.

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