Good Clinical Practice
ICH E6(R3) Good Clinical Practice principles, investigator responsibilities, participant rights and safety, and reliable clinical-trial data.
About GCRP
Georgia Clinical Research Partners is being built to support responsible clinical research across the communities we serve.

Our purpose
GCRP is a standalone clinical research organization focused on the careful coordination of patients, physicians, investigators, sponsors, and CROs. Our name reflects the standard we bring to every interaction: GCP is in our name.
Our investigators are board-certified physicians with substantial experience in their respective medical specialties. They pair clinical judgment with research oversight, supported by clinical research coordinators focused on participant communication, protocol execution, documentation, and follow-through.
We believe good research operations begin with clear communication, respect for informed choice, and disciplined execution. Those principles guide how we explain studies to potential participants and how we work with research partners.
Research quality standards
Our SMO and CRC practices are structured around the standards expected of high-quality research sites, applied as appropriate to each protocol and study.
ICH E6(R3) Good Clinical Practice principles, investigator responsibilities, participant rights and safety, and reliable clinical-trial data.
Applicable FDA requirements—including 21 CFR Parts 50 and 56 and, when relevant, Parts 312 or 812—together with IRB oversight, protocol adherence, safety reporting, and privacy safeguards.
Contemporaneous source documentation, ALCOA+ data-integrity principles, trained and appropriately delegated staff, monitoring readiness, issue escalation, and corrective-action discipline.
What guides us
Plain-language information that supports questions and informed decisions.
Participant dignity, privacy, and voluntary choice at every stage.
Careful processes, candid communication, and responsible follow-through.