Guidance

Wholesalers & manufacturers guidance following agreement of the Windsor Framework

Actions QPs, RPis and RPs need to take following agreement of the Windsor Framework

From:
Medicines and Healthcare products Regulatory Agency
Published
12 September 2024
Last updated
20 February 2025 — See all updates

Documents

WholesalersWholesalers' &and manufacturersmanufacturers' guidance following agreement of the Windsor Framework

HTML

Windsor Framework disapplication of EU falsified medicines directive Q&A

PDF, 276 KB, 6 pages

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Windsor Framework wholesaler and manufacturer Q&A

PDF, 323 KB, 9 pages

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Details

ThisGuidance guidance is designed to support manufacturers and wholesale dealers authorised by the MedicinesMHRA and Healthcare products Regulatory Agency (MHRA) and the associated Qualifiedqualified Personspersons (QPs), Responsibleresponsible Personspersons (RPs) and Responsibleresponsible Personspersons for Importimport (RPis), in order to implement the arrangements of the Windsor Framework for human medicines.

Updates to this page

Published 12 September 2024
Last updated 20 February 2025 + show all updates

  1. Updated the document Wholesalers & manufacturers guidance following agreement of the Windsor Framework to add Windsor Framework Wholesaler and Manufacturers Q&A and FMD Q&A

  2. First published.

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