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APACMed

The Voice of MedTech in Asia

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Home » Public Resources » Regulatory Affairs » Page 3

Posts in category: Regulatory Affairs

The_Necessity_for_Regional_Regulatory_Reliance_in_ASEAN

The Necessity for Regional Regulatory Reliance in ASEAN

May 25, 2022
by apacmed
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Advamed-APACMed joint Position Letter - Industry concerns on Draft Presidential Regulation on Halal Certification of Medicine, Biological Products and Medical Devices

Advamed-APACMed joint Position Letter: Industry concerns on Draft Presidential Regulation on Halal Certification of Medicine, Biological Products and Medical Devices

May 4, 2022
by Cissy Chen
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Understanding Digital Health Regulations For MedTech In Asia Pacific Markets

Understanding Digital Health Regulations For MedTech In Asia Pacific Markets

March 1, 2022
by Cindy Pelou
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Screenshot 2022-02-25 at 6.39.33 PM

APACMed Digital Health Webinar – 亚太医疗技术协会数字医疗系列研讨会 -中国数字健康法规专题

February 25, 2022
by Cindy Pelou
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SAMD_regulations

Guidance on SaMD Regulations – Lifecycle Approach: An APACMed India Digital Health Centre of Excellence Initiative

January 31, 2022
by Cissy Chen
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RA_05

APACMed Position Letter on Unique Device Identifier (UDI) for Medical Devices in India

January 31, 2022
by Cissy Chen
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Paper Launch – Digital Health Regulation in Asia-Pacific - China and Korea

Paper Launch – Digital Health Regulation in Asia-Pacific: China and Korea

January 28, 2022
by Cindy Pelou
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:content:uploads:2021:10:Digital-Health-Regulation-in-India_Position-Paper

Digital Health Regulation in India Position Paper

October 12, 2021
by Cissy Chen
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Screenshot 2021-09-23 at 5.24.02 PM

Digital Health Regulation In Asia-Pacific: China and Korea

September 23, 2021
by Cindy Pelou
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RA_03

APACMed Position Letter on Halal Regulations in Indonesia

September 14, 2021
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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