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UK MHRA Guidance: Clinical Trials: How to Modify a Clinical Trial Approval
Clinical trials may need to be changed during their lifecycle because of developments in trial design, participant safety, medicines, scientific information, or trial administration. The Medicines and Healthcare products Regulatory Agency (MHRA) has published guidance, Clinical trials for medicines: modifying a clinical trial approval, explaining the different types of modifications that can be made to a clinical trial approval. The amended Clinical Trials Regulations took fu

Sharan Murugan
7 hours ago7 min read
