Identification of Medicinal Products

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Members
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Members
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  • ANVISA, Brazil
  • APEC
  • ASEAN
  • CECMED, Cuba
  • COFEPRIS, Mexico
  • CPED, Israel
  • EAC
  • EC, Europe
  • EDA, Egypt
  • FDA, United States
  • Health Canada, Canada
  • HSA, Singapore
  • JFDA, Jordan
  • MHLW/PMDA, Japan
  • PAHO/PANDRH
  • Roszdravnadzor, Russia
  • SADC
  • SAHPRA, South Africa
  • SFDA, Saudi Arabia
  • Swissmedic, Switzerland
  • TFDA, Chinese Taipei
  • TGA, Australia
  • TITCK, Türkiye
  • WHO 
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Scope (Mandate) and Objectives
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Scope (Mandate) and Objectives
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  • The IDMP Working Group objectives: 

    • Ensure the awareness and understanding of the standards of the IDMP standards more globally by pharmaceutical regulators 

       

    • Clarify how and why these standards can add value to regulator business processes to improve the quality and effectiveness of shared regulatory functions, 

       

    • Share strategies and experiences for their successful and consistent implementation.

       

  • Mandate document endorsed November 2016

     

Key Deliverables:

 

  • Outreach and communication on IDMP

     

  • Publish Frequently Asked Questions (Version 6)

     

  • Publication of documents in relation to the activities identified in the Scope of the WG and sharing of the public documentation produced by the early adopters for their regional/national implementation.
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Work in Progress
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Work in Progress
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The working group has an on-going project, preparing the FAQ Document Version 7 which will be updated and is considered a living document.

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Work Products
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Links to Other Facts
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Links to Other Facts
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