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APACMed

The Voice of MedTech in Asia

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Home » Public Resources » Regulatory Affairs

Posts in category: Regulatory Affairs

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Advancing Software as a Medical Device Regulations in Asia-Pacific

August 20, 2025
by Cissy Chen
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Regulatory Reliance Pathways Tracker

July 10, 2025
by Cissy Chen
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APACMED–NUS Workshop on advanced medical device regulation

June 18, 2025
by Cissy Chen
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Protected: APACMed Regulatory Intelligence Bulletin: January – December 2025

January 31, 2025
by Cissy Chen
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Regulatory Landscape of Laboratory Developed Tests (LDT) in APAC

January 8, 2025
by Cissy Chen
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Risk-Based Change Management for Registered Medical Devices

November 19, 2024
by Cissy Chen
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Value-Based Market Access Symposium in Japan

October 25, 2024
by Cissy Chen
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APACMed Position Paper on Post-Market Surveillance and Vigilance

October 24, 2024
by Cissy Chen
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DMPAW-kOREA

Korea’s Digital Medical Products Act Webinar

September 27, 2024
by Cissy Chen
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Hand using laptop computer with virtual screen and document for online approve paperless quality assurance and ERP management concept.

Towards MedTech Efficiency & Sustainability through e-Label & e-IFU

September 3, 2024
by Cissy Chen
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Who We Are

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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