Transcription of Monitoring & Auditing of Clinical Trials
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Monitoring & Auditing of Clinical Trials
Monitoring & Auditing of Clinical TrialsDeveloped by Center for Cancer Research, National Cancer Institute, NIHS upported by the CTN SIG Leadership GroupObjectivesGuidelines suggest that following the good Clinical research practice of Monitoring / Auditing should be done for the reasons previously stated. That is why, whether you participate in FDA regulated research or not, there should be some local policies and procedures in place for the routine evaluation ( , an audit) of a Clinical the conclusion of this module you will be able to: Describe the purposes and regulations related to Monitoring of Clinical Trials . Discuss the difference between Monitoring and Auditing . Describe three types of sponsored study visits.
• Describe the purposes and regulations related to monitoring of clinical trials. • Discuss the difference between monitoring and auditing. • Describe three types of sponsored study visits.
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