The IRB determines, for each protocol it reviews, which of the following elements and disclosures must be included in the informed consent process. Investigators can avoid delay in the review process ...

1. Investigators have not completed required CITI training courses/ modules. See the HRPP Required Training webpage for guidance. Note that if you have taken a CITI course elsewhere, you must ...

In order to address the specific details and regulatory requirements present in a retrospective medical chart review, the UB IRB recently created a new Protocol template: the HRP-503R. In order to ...

GREENVILLE, S.C.--(BUSINESS WIRE)--Avallano is launching ProtocolCopilot™, an innovative AI-driven clinical research protocol assistant designed to transform the way biopharmaceutical companies and ...