Скачать или смотреть Who Oversees Patient Safety In Clinical Trials?

Ever wondered who stands guard over patient well-being during groundbreaking medical research? This video delves into the critical systems and organizations responsible for ensuring patient safety in clinical trials, a cornerstone of ethical drug development and new treatment exploration.

Discover the key players and processes involved in safeguarding clinical trial participants:
► The crucial role of Institutional Review Boards (IRBs) or Ethics Committees in reviewing and approving research protocols.
► How regulatory bodies like the FDA or EMA provide oversight and enforce strict guidelines for trial conduct.
► The continuous monitoring by Data Safety Monitoring Boards (DSMBs) to assess adverse events and trial progress.
► The importance of informed consent and patient rights in clinical research.
► The responsibilities of sponsors, investigators, and clinical research organizations (CROs) in maintaining patient safety.


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