The UK’s medicines regulator has given an update on what drugmakers can expect when it comes to registration of clinical trials, in the event of a "no-deal" Brexit.
The advice follows earlier guidance provided to help companies plan for what analysts say could be a highly disruptive period for the industry.
The Medicines and Healthcare products Regulatory Agency (MHRA) makes clear the guidance will only apply in the event of the UK leaving the EU without a negotiated settlement or withdrawal period.
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