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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

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Medical Device Regulations in APAC: Examples from Singapore, South Korea, India, Japan and Australia

October 12, 2022
by Shawn Lim
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Unlocking the Value of Quality Next-Generation Sequencing in APAC

September 26, 2022
by Cindy Pelou
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APACMed – ADVAMED Position Paper on Standards

July 4, 2022
by apacmed
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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 admin
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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 Melissa
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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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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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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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