GCP Training

Good Clinical Practices (GCP) training — ICH E6 R2 fundamentals, sponsor / investigator / IRB roles, informed consent, and audit-readiness.

What is GCP Training?

This programme makes ICH-GCP (E6 R2) something you can apply, not just recite. Whether you're heading into a CRO, a sponsor, an investigator site, or an ethics committee, GCP fluency is non-negotiable — this training builds it cleanly.

What you will learn

ICH E6 R2 structure — sections, principles, key updates from R1
Roles and responsibilities — Sponsor, Investigator, IRB / IEC, Monitor
Informed consent — full discussion, common findings, vulnerable populations
Source data, source documents, and ALCOA+ in clinical trials
Trial Master File (TMF) and Investigator Site File (ISF) discipline
Monitoring, audits, and inspection-readiness

Who this is for

Students and early-career professionals from life sciences, pharmacy, nursing, biotechnology, and clinical research heading into CRO, sponsor, site, or ethics-committee roles.

What you take away

NTHRYS training certificate detailing GCP scope
Working understanding of GCP as it actually shows up at sites and sponsors
A capstone GCP-applied case study deliverable
A direct profile for CRC, CRA, CDM, and clinical-operations roles

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