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Posts in category: Regulatory Affairs (Member Restricted)

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APACMed Regulatory Intelligence Bulletin: January – December 2022

February 14, 2022

by Cissy Chen

MDA’s Re-registration process, its challenges and recommendation by APACMed

November 30, 2021

by Cissy Chen

Regulatory Reliance For The Registration Of Medical Devices In Asia Pacific

by Cissy Chen

Post Market Surveillance for RA Professionals

India Session On Post Market Surveillance for RA Professionals

by Cissy Chen

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HIMSS round table with IMDRF regulators – Development of regulatory frameworks for SaMDs

by Cindy Pelou

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AHWP/ GHWP Regulatory Capacity Building Paper Launch- Medical Device Regulatory Training Curriculum for Industry Professionals

by Cissy Chen

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APACMed India Regulatory Capacity Building – Session on EU MDR

February 19, 2021

by Cissy Chen

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Regulatory Advances in Artificial Intelligence/Machine Learning

February 11, 2021

by Cissy Chen

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MedTech Regulatory Intelligence Watch: January – December 2021

February 2, 2021

by Cissy Chen

APACMed Regulatory Capacity Building Unique Device Identifier UDI Module 1 – 3

October 9, 2020

by Cissy Chen