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Post# of 705651
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Re: ae kusterer post# 661612

Friday, 01/05/2024 8:58:36 AM

Friday, January 05, 2024 8:58:36 AM

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"IRP allows us to access the expertise of trusted regulatory partners, who have already authorised products. In return, our partners can consider applications based on MHRA authorisations, creating a ‘win-win’ for regulators, developers of innovative treatments, and patients"

So, when we receive MHRA approval, we can apply under the IRP for submission to IRP partners

"At launch, the MHRA will partner with regulators in Australia, Canada, Japan, Singapore, Switzerland and the USA, as well as the European Medicines Agency, individual EU member states and those in the EEA (European Economic Area)".

https://www.gov.uk/government/news/mhras-new-international-recognition-procedure-irp-goes-live-from-1-january-2024
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