# Clinical Research — markdown corpus

> US clinical research regulatory compliance: FDA human subjects protection and investigational new drug/device rules under 21 CFR Parts 50, 56, 312, and 812, the ICH E6 Good Clinical Practice guideline, OHRP guidance on IRB oversight, and ClinicalTrials.gov registration and reporting requirements — grounded exclusively in fda.gov, ich.org, hhs.gov/ohrp, and clinicaltrials.gov. Regulatory reference only.

License: CC BY 4.0 — https://creativecommons.org/licenses/by/4.0/
Attribution: Source: MIND (m-i-n-d.ai)
Hub: https://www.m-i-n-d.ai/minds/clinical-research
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