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        • Good Regulatory Practices
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AdvaMed Applauds Summit of the Americas’ Focus On Importance of Business Ethics and Good Regulatory Practices

Home » AdvaMed Applauds Summit of the Americas’ Focus On Importance of Business Ethics and Good Regulatory Practices

The Advanced Medical Technology Association (AdvaMed) issued this press release following the recent conclusion of the VIII Summit of the Americas in Lima, Peru on April 14.

April 20, 2018

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  • About
    • Terms of Reference
    • Members
    • Technical Secretariat
    • Executive Committee
    • Join the Coalition
    • Contact Us
  • Coalition Action
    • Events
    • Positions by Country
    • Positions by Topic
    • Action Plan (2020-2025)
    • Multilateral Engagement
  • Policy
    • International Standardization
      • Standardization and Conformity Assessment
      • Standards Development Organizations, Committees and Standards for Medical Technology
        • ISO/IEC
        • ASTM International
        • AAMI
        • CLSI
        • MITA
        • GMDN Agency
        • National Standards Bodies from the Americas
      • Use of International Standards by Medical Device Regulators
        • FDA – Use of International Standards
    • Medical Device Sector Regulatory Convergence
      • World Health Organization Documents
        • WHO Global Model Regulatory Framework for Medical Devices including In Vitro Diagnostic Medical Devices
        • Good Regulatory Practices
        • Good Reliance Practices
        • Post Market Surveillance
      • International Medical Device Regulators Forum
        • IMDRF Essential Principles of Safety and Performance of Medical Devices and IVD Medical Devices
        • IMDRF Documents
          • SaMD
          • Clinical Investigation
      • Medical Device Single Audit Program (MDSAP)
    • Good Regulatory Practices
      • OECD
      • APEC
      • WTO/TBT
      • WTO Agreements Implementation by Country
      • Regional & Bilateral Trade Agreements / GRP & TBT
        • USMCA
        • Pacific Alliance
      • ABD/IDB
      • Central Regulatory Coordination
    • Transparency & Trade
      • Relationship Between Regulatory and Transparency
      • Trade
  • Training
    • Policy Training
    • Regulator Sessions
    • International Symposia
  • Projects
    • Standards Alliance
      • Standards Alliance 1.0
        • Tier 1 – Good Regulatory Practices (GRP = Regulatory Coherence)
          • Colombia
          • Costa Rica
          • Mexico
          • Peru
          • United States
          • All Countries
          • Tier 1 – Global Benchmark Documents – Overarching Good Regulatory Practices and Technical Barriers to Trade Requirements
        • Tier 2 – Medical Device Sector-Specific Good Regulatory Practices, Technical Regulations, Standards, And Conformity Assessment
          • Tier 2 – Global Benchmark Documents – Medical Device Sector Regulatory Frameworks, GRPs, Regulations, Standards, Conformity Assessment mechanisms
      • Standards Alliance Phase 2 COVID-19 Medical Device Regulatory Convergence Project (MDRC)
        • Africa
        • Latin America
        • Southeast Asia
  • Quick Links
    • Medical Device Regulatory Authorities
    • WHO Medical Devices Web Page
    • WHO In vitro diagnostics
    • GMTA collaboration plan with WHO 2021-2023
    • PAHO Medical Devices Web Page
    • Central Regulatory Coordination Bodies
    • National Standards Bodies from the Americas
    • WTO/TBT National Enquiry Points
    • Harmonized System (HS) Codes for MedTech
    • WTO/TBT Notifications on Medical Technology
    • Open Public Consultations
  • COVID-19
    • Coalition Recommendations to the IDB
    • Coronavirus – Use of Antibody Tests
    • Brazil Response
    • Colombia Response
    • Mexico Response
    • United States of America Response
  • News