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Clinical trials involving investigational medicinal products (CTIMPs) in the UK are governed by the Medicines for Human Use (Clinical Trials) Regulations 2004 (as amended), with safety reporting requirements set out in MHRA and Health Research Authority (HRA) guidance
Freezing temperatures destroy the delicate peptide structure of the medication
Philipose, et al., 'Once-Monthly Maridebart Cafraglutide for the Treatment of Obesity - A Phase 2 Trial', N
This guide will walk you through obtaining these reports and then using them to add the client's data to CCH Axcess
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