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ATMP Engage PPI Directory

The PPI Directory contains patient and public involvement (PPI) resources for developers of cell and gene therapies, including toolkits, guidelines, advice, templates and case studies.

PPI Directory

PPI Themes
Research Field
Organisation Type
Development Stage
Audience
Country
Content Type
    Showing 5 of 171 results.
    Page 19 of 35
    2014

    Revised framework for interaction between the European Medicines Agency and patients and consumers and their organisations

    Generic PPI framework by the European Medicines Agency

    Research Field

    • Other

    Organisation Type

    • Regulatory Body

    Development Stage

    • Regulatory Approval

    Audience

    • Researchers/Developers
    • Public/Patients

    Country

    • Europe

    Content Type

    • Resource
    2020

    EMA Regulatory Science to 2025 - strategic reflection

    Report reflecting on the EMA's regulatory framework by the European Medicines Agency

    Research Field

    • Other

    Organisation Type

    • Regulatory Body

    Development Stage

    • Regulatory Approval

    Audience

    • Researchers/Developers
    • Public/Patients

    Country

    • Europe

    Content Type

    • Resource

    Advanced Therapy Classification

    Classification of ATMPs by the European Medicines Agency

    Research Field

    • ATMP/Gene Therapy Development

    Organisation Type

    • Regulatory Body

    Audience

    • Researchers/Developers
    • Public/Patients
    • Charity Sector
    • Industry
    • Other groups

    Country

    • Europe

    Content Type

    • Resource
    2018

    Guideline on safety and efficacy follow up and risk management of ATMPs

    Report on guidance on long term follow up for ATMPs by the European Medicines Agency

    Research Field

    • ATMP/Gene Therapy Development

    Organisation Type

    • Regulatory Body

    Development Stage

    • Regulatory Approval

    Audience

    • Researchers/Developers

    Country

    • Europe

    Content Type

    • Resource
    2018

    Procedural advice on the evaluation of advanced therapy medicinal product in accordance with Article 8 of Regulation (EC) No 1394/2007

    Document outlining the procedure on ATMP evaluation by European Medicines Agency

    Research Field

    • ATMP/Gene Therapy Development

    Organisation Type

    • Regulatory Body

    Development Stage

    • Regulatory Approval

    Audience

    • Researchers/Developers

    Country

    • Europe

    Content Type

    • Resource