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What really made me take this course in the first place was the flexibility of time. As busy as I am, I try to find educational courses that will be suitable and will fit in my daily routine without making me sacrifice other projects and initiatives.

Kemal Senniar

How to report Adverse Events to IRBs

Accreditation: Bii approved
CPD: 0 CPD points

Duration: 3 hours
Certificate: No

Free course

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The Adverse Event Reporting to Institutional Review Boards/Independent Ethics Committees (Human Subject Protection) online training provides insight into important aspects of adverse event reporting, and expert advice on what must be done for human subject protection to be improved in clinical trials.It provides a better understanding of how adverse events should be treated and an insight into the competent authorities and the proper ways to report to them.

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Testimonials

How to report Adverse Events to IRBs

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