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Brexit: The legal and regulatory impact on supply chain and pharmacovigilance

Post thumbnail Brexit: The legal and regulatory impact on supply chain and pharmacovigilance

The UK will withdraw from the EU on 29 March 2019. By 1 August 2018, no agreement had been reached on a transitional arrangement to soft en the impact of Brexit. The European Commission and the European Medicines Agency (EMA) have taken a strict position on Brexit, considering the UK to be a third country from 30 March 2019, as reflected in the Q&A document published in its third version in June 2018. This article spells out the impact of that scenario on the pharmaceutical supply chain and pharmacovigilance, but also looks at the more positive scenario – namely in case the draft “Withdrawal Agreement” is ratifi ed by the UK and EU in time for Brexit. In the “hard Brexit” scenario, companies need to have transferred licences in due time, have adapted their supply chains and processes and have re-located pharmacovigilance operations and persons.

In the case of a transitional regime where EU law continues to apply (“soft Brexit”), no such drastic measures may be necessary. However, the continued uncertainty means that – to some degree – hard Brexit has already happened for the pharmaceutical industry in Europe.


Published on: November, 2018
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    publication by

    Susan Salako thumbnail
    Susan Salako
    Regulatory Scientist
    Peter Embley thumbnail
    Peter Embley
    Senior Director Regulatory Sciences