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APACMed

The Voice of MedTech in Asia

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Home » Public Resources » Regulatory Affairs » Page 2

Posts in category: Regulatory Affairs

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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Mastering the Regulatory Landscape for AIML-enabled SaMD

Mastering the Regulatory Landscape for AI/ML-enabled SaMD

June 4, 2024
by Devya Bharati
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Indonesia Halal Policy for Medical Technologies – An Industry Perspective

March 26, 2023
by Cissy Chen
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Medical Device Regulations in APAC: Examples from Singapore, South Korea, India, Japan and Australia

October 12, 2022
by Cissy Chen
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NGS_paper_webcover

Unlocking the Value of Quality Next-Generation Sequencing in APAC

September 26, 2022
by Cindy Pelou
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ADVAMED Cover

APACMed – ADVAMED Position Paper on Standards

July 4, 2022
by apacmed
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Sri Lanka cover

APACMed Position Paper – Pathway for Harmonizing the Medical Devices Registration Process in Sri Lanka

July 4, 2022
by apacmed
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FAQ Med Equipment

FAQs – Medical Equipment Regulations in India

July 4, 2022
by apacmed
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Regulatory Transformation Symposium 2022 – Event Recordings

June 8, 2022
by Cissy Chen
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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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