Serious Adverse Event Reporting for Investigators

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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.

For more insight into our world of Clinical Research, and to be sure not to miss a thing,

It’s all about the mindset, the GCP-Mindset 💡

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Thank you, I have a question regarding the reporting of adverse evens to the authority, Do they have to report all AEs? Or just SAE and DD to the authority? And what is the period of time for reporting for all types of AEs?

Alhajlan

Researchers are not required to account of disclosure of protected health information when

geethamk

Does coordinators report SAE or write it? She mentioned Investigators, not coordinators.

christineokparaki

This Lady looks like she was made by AI

MorpheousIlango

Serious Adverse Event Reporting for Investigators

Serious Adverse Event Reporting for Investigators

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