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CRUK, ECMC and UK Radiopharmacy Taskforce (CERT

CERT aims to provide a common understanding of regulatory requirements for clinical trials that involve radiopharmaceuticals. At this link you will find step by step guidance and advice related to the set-up of clinical trials, associated quality systems and regulatory requirements when using molecular radiopharmaceutical Investigational Medicinal Products

Click on the link below to view the CERT resources area