Before IRB Review: Additional Requirements
-
Clinical protocols in the NIH Intramural Research Program that require IRB approval must undergo scientific review at the Institute/Center (IC) level…
-
This page explains the management of real or apparent conflicts of interest for investigators conducting NIH Intramural clinical research, and/or whe…
-
NIH technology transfer helps move discoveries and inventions from NIH labs to public and private sectors for commercialization and public benefit.
-
Scans, tests, and procedures involving radiation that are specified in the protocol are considered research procedures by the Institutional Review Bo…
-
The NIH Institutional Biosafety Committee (IBC) reviews and approves research protocols involving rDNA techniques or potentially infectious/toxic mat…
-
The PRIA is a prospective review to ensure that the Clinical Center (CC) has the expertise, equipment, and resources needed to successfully conduct c…
-
The Human Fetal Tissue (HFT) ancillary review ensures that HFT is used only when scientifically justifiable.