Home » All IRBs Will Soon Be Required to Register Electronically
All IRBs Will Soon Be Required to Register Electronically
All institutional review boards (IRBs) for clinical trials in the U.S. will be required to register electronically with HHS under final rules issued simultaneously by the FDA and the Office for Human Research Protections (OHRP) and set to take effect July 14. The purpose of the new rules is to make it easier to inspect IRBs and provide them with information, according to the FDA and OHRP.
Clinical Trials Advisor
Clinical Trials Advisor
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