Tuesday, September 15, 2020

Explainer: On how Serious Adverse Events (SAE) of clinical trials are reported, participant compensation

Explainer: On how Serious Adverse Events (SAE) of clinical trials are reported, participant compensation The investigator should report all serious adverse reactions to the drug regulatory body Drug Controller General of India (DCGI), sponsor of the trial and the concerned Ethics Committee that approved the trial protocol within 24 hour of occurrence.

from Moneycontrol Business News https://ift.tt/2H3fzpW
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