Researchers and study staff conducting research subject to ICH-GCP requirements must ensure training is completed by February 20, 2026.
ClinicalTrials.gov is a public registry of research studies involving human subjects. ClinicalTrials.gov is the result of a federal law requiring that clinical trials be registered to improve public access to information about clinical research, promote public trust in research, and inform future research.
The trainings listed below are a non-exhaustive list of required trainings related specifically and solely to OEC areas.
IND Sponsor-Investigators are expected to submit brief annual reports of the progress of the investigations conducted under their IND application within 60 days of the anniversary date that the application went into effect.
