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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 admin

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

November 30, 2021

by admin

Regulatory Reliance For The Registration Of Medical Devices In Asia Pacific

by admin

Post Market Surveillance for RA Professionals

India Session On Post Market Surveillance for RA Professionals

by admin

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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 admin

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APACMed India Regulatory Capacity Building – Session on EU MDR

February 19, 2021

by admin

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Regulatory Advances in Artificial Intelligence/Machine Learning

February 11, 2021

by admin

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MedTech Regulatory Intelligence Watch: January – December 2021

February 2, 2021

by admin

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

October 9, 2020

by admin

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APACMed provides a unifying voice for the medical devices and in-vitro diagnostics industry in Asia Pacific. Founded in 2014, APACMed strives to promote innovation and impact policy that advances healthcare access for patients.

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