New funding announced yesterday for the UK Medicines and Healthcare products Regulatory Agency will be used to develop a “thorough but shortened process” to speed up the approval of innovative UK-developed products such as cancer vaccines and AI-based therapeutics for mental health conditions.
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An injection of new money should provide something of a shot in the arm for the UK’s drugs regulator as it deals with post-Brexit realities.
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Recent and upcoming US FDA advisory committee meetings and a summary of the topics covered.