This week's edition of Life Sciences weekly highlights includes an MLex analysis of AI model providers receiving confirmation of delays to the EU Code of Practice intended to help them comply with the EU AI Act. Also included is news that MedTech Europe developed a series of concise one-pagers designed to support the effective implementation of the MDR and the IVDR, the European Commission published an updated mandatory manufacturer incident report (MIR) under the MDR/IVDR, the Medicines for Human Use (Clinical Trials) Regulations 2004, SI 2004/1031 will reform the UK legislation for clinical trials, responding to the needs of the sector to deliver a more streamlined and flexible regulatory regime, and the EMA revised its policy on access to EudraVigilance data for medicinal products for human use.
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