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Regulatory Convergence
Inter-American Coalition
Regulatory Convergence
  • English
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  • About
    • Medical Device Definition
    • Terms of Reference
    • Members
    • Technical Secretariat
    • Executive Committee
    • Multilateral Engagement
    • Join the Coalition
    • Contact Us
  • Coalition Action
    • Action Plan (2020-2025)
    • IACRC Positions
    • IACRC Meetings
  • Regulatory Policies
    • International Obligations on GRP
      • OECD
      • WTO
      • Regional & Bilateral Trade Agreements focusing on Regulatory Convergence and GRP
      • Implementation of GRP by Country
      • ABD/IDB
      • Central Regulatory Coordination
    • Medical Device Sector Regulatory Convergence
      • World Health Organization Documents
      • International Medical Device Regulators Forum (IMDRF)
        • IMDRF Essential Principles of Safety and Performance of Medical Devices and IVD Medical Devices
        • IMDRF Documents
          • SaMD
          • Clinical Investigation
        • IMDRF Meetings
      • Medical Device Single Audit Program (MDSAP)
      • How International Standards are applied by Medical Device Regulators
    • International Standards on Medical Device applied by Countries
      • ISO/IEC
      • AAMI
      • ASTM International
      • CLSI
      • MITA
      • National Standards Bodies from the Americas
  • Capacity Building
    • Training Sessions
    • External Participation of the IACRC
  • Projects
    • Standards Alliance
      • Standards Alliance 1.0
        • Tier 1
        • Tier 2
      • Standards Alliance 2.0
  • Quick Links
    • Medical Device Regulatory Authorities
    • WHO Medical Devices Web Page
    • PAHO Medical Devices Web Page
    • National Standards Bodies from the Americas
    • Central Regulatory Coordination Bodies
    • ePing
    • HS and HTS codes for Medical Devices (The MD export codes for use on the ePing site)
  • News
  • About
    • Medical Device Definition
    • Terms of Reference
    • Members
    • Technical Secretariat
    • Executive Committee
    • Multilateral Engagement
    • Join the Coalition
    • Contact Us
  • Coalition Action
    • Action Plan (2020-2025)
    • IACRC Positions
    • IACRC Meetings
  • Regulatory Policies
    • International Obligations on GRP
      • OECD
      • WTO
      • Regional & Bilateral Trade Agreements focusing on Regulatory Convergence and GRP
      • Implementation of GRP by Country
      • ABD/IDB
      • Central Regulatory Coordination
    • Medical Device Sector Regulatory Convergence
      • World Health Organization Documents
      • International Medical Device Regulators Forum (IMDRF)
        • IMDRF Essential Principles of Safety and Performance of Medical Devices and IVD Medical Devices
        • IMDRF Documents
          • SaMD
          • Clinical Investigation
        • IMDRF Meetings
      • Medical Device Single Audit Program (MDSAP)
      • How International Standards are applied by Medical Device Regulators
    • International Standards on Medical Device applied by Countries
      • ISO/IEC
      • AAMI
      • ASTM International
      • CLSI
      • MITA
      • National Standards Bodies from the Americas
  • Capacity Building
    • Training Sessions
    • External Participation of the IACRC
  • Projects
    • Standards Alliance
      • Standards Alliance 1.0
        • Tier 1
        • Tier 2
      • Standards Alliance 2.0
  • Quick Links
    • Medical Device Regulatory Authorities
    • WHO Medical Devices Web Page
    • PAHO Medical Devices Web Page
    • National Standards Bodies from the Americas
    • Central Regulatory Coordination Bodies
    • ePing
    • HS and HTS codes for Medical Devices (The MD export codes for use on the ePing site)
  • News

Coalition Action

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Coalition Action Plan for 2020-2025

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Coalition Action
  • IACRC Positions
  • Positions by Country
  • Positions by Topic
  • Action Plan (2020-2025)
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