Basics - Part 14 - SUSAR Suspected Unexpected Serious Adverse Reaction
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What everybody should know about Clinical Trials!
Without clinical trials, we wouldn’t have any vaccines, treatments for cancer, heart disease, diabetes and many others. What should everybody know about Clinical Trials? How are pharmaceuticals and medical devices developed? This is our new video of our series about the basics of clinical trials to give you some answers. Part 14 - SUSAR Suspected Unexpected Serious Adverse Reaction is presented by our expert Kelsey Crossman.
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@fredrikh9299 2 жыл бұрын
Thank you!
@dongwang1801 10 ай бұрын
Thanks!
@varunsharma7521 3 жыл бұрын
Well explained, thank you 👍
@GCPMindset 2 жыл бұрын
Glad you liked it
@okellomaurice6073 Жыл бұрын
Given the timelines for reporting of the SUSARs by the sponsor, how long should it take for the sites to report to the sponsor? Especially those sites which are multinational.
@Lamp141 2 жыл бұрын
What are the requirements for cross reporting of foreign SUSAR?
@vivekrakha5295 3 жыл бұрын
Good video
@GCPMindset 3 жыл бұрын
Thanks
@dheerajkanoj7066 3 жыл бұрын
What is casuality for SUSAR?
@sindhusetty2724 Ай бұрын
Can you pls tell me like if a serious adverse event was unexpected as per IB and expected as per ccds or rsi can we consider as susar, pls tell me
@GCPMindset Ай бұрын
The reference safety information should be defined before the start of the study. Usually, the reference safety information is a specific section in the IB. If the event is not listed in this section, the event is considered unexpected.
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