Guidance

Further guidance note on the regulation of medicines, medical devices and clinical trials in a no-deal Brexit

Information for stakeholders so you can make informed plans and preparations in the event of leaving the EU with no deal.

• From: Medicines and Healthcare products Regulatory Agency
• Published: 3 January 2019
• Last updated: 3 September 2019
  Show all updates

  1. 3 September 2019

     Updating of four dates.

  2. 8 August 2019

     We have removed some outdated information, reflecting the publication of more specific guidance in some areas. We have also removed some background information.

  3. 26 February 2019

     Added link to new guidance document about regulating medical devices in the event of a no deal scenario.

  4. 4 January 2019

     In section 3.6, 'Regulatory requirements for Investigational Medicinal Product (IMP) for trials', we have replaced the phrase 'the EU's current position is that testing of IMP should be undertaken within the EU/EEA to 'the EU’s current position is that QP certification of IMP must be undertaken within the EU/EEA'.

  5. 3 January 2019

     First published.

This publication was withdrawn on 31 January 2020

For current information on medicines, medical devices and clinical trials see MHRA services and information

Documents

Further guidance note on the regulation of medicines, medical devices and clinical trials if there’s no Brexit deal

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Details

This guidance is intended to update stakeholders on the UK’s proposed arrangements for the regulation of medicines, medical devices and clinical trials.

See the full list of no deal guidance published by the MHRA.