Following announcement in May of the new scheme to replace the current EC Decision Reliance Procedure (ECDRP) on 1 January 2024, this guidance informs the sector on how they can use the scheme to apply for a medicine licence in the UK, following approval by trusted regulatory partners in Australia, Canada, the European Union, Japan, Switzerland, Singapore, and the United States.
This means that patients will have faster access to safe, effective cutting-edge medicines through our review and by leveraging the expert decision-making of our regulatory partners to streamline assessments of specific products, while maintaining the power of the MHRA as a sovereign regulator to scrutinise each application and the authority to reject them if the evidence provided is considered insufficiently robust…
