Article summary
The Medicines and Healthcare products Regulatory Agency (MHRA) and National Institute for Health and Care Excellence (NICE) outlined new regulatory processes on 17 March 2025 as part of wider government reforms. From July 2025, MHRA will permit point-of-care manufacturing of personalised medicines, while NICE aims to complete 60% of Technology Appraisals within 240 working days by 2025/26. The regulators will launch an integrated scientific advice service and implement concurrent marketing authorisation and technology appraisal processes to reduce approval times for new medicines.
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