MCRA RESOURCE CENTER

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CLINICAL

The purpose of the GCP is to provide guidance on good clinical practice and the conduct of clinical trials. These guidance documents are enforceable by the FDA and require that all parties involved in a clinical trial to be held accountable for the conduct of the study.


 
 
 

GCP UPDATES

FDA Office of Good Clinical Practices

FDA Clinical Trials and Investigational Device Exemption (IDE)

CDRH Office of Compliance - Bioresearch Monitoring Program

Consent form template