UK Avoids 'Cliff Edge' By Extending EU Drug Approval Reliance Procedure

The UK drugs regulator says it needs to make sure that companies do not “deprioritize” GB approval applications while a new “international reliance framework” is being developed.

Plenty of capsules and pills laying on a flag of Great Britain
The UK MHRA will continue to allow reliance on EU drug approvals for another year • Source: Shutterstock

The UK Medicines and Healthcare products Regulatory Agency (MHRA) has extended by one year the streamlined procedure that allows pharmaceutical companies to gain faster Great Britain marketing authorizations based on approval recommendations made by the European Medicines Agency.

The European Commission Decision Reliance Procedure (ECDRP) was introduced in response to concerns that after Brexit, companies might delay new drug submissions to the MHRA in favor of an EU

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