Start with our free Good Clinical Practice (GCP) track—from beginner to ICH E6(R3) certified. Then advance through specialized career tracks designed for clinical research professionals.
We distilled ICH E6(R3) into nine comprehensive modules. Each combines narrative storytelling, regulatory interpretation, and practical worksheets so you can apply Good Clinical Practice the moment you finish.
Total Duration
6 hours
Self-paced, progress saved
Assessments
100+
Scenario-based questions
Built with senior CRAs, quality leads, and principal investigators.
Begin your ICH E6(R3) journey with a comprehensive overview of Good Clinical Practice—its history, global adoption, and why it matters for participant safety and data integrity.
Understand the distinct obligations of every stakeholder—investigators, sponsors, CROs, and ethics committees—and how each safeguards participant rights under E6(R3).
Master the informed consent process—from initial approach through ongoing re-consent—with special attention to vulnerable populations and E6(R3) documentation requirements.
Learn protocol adherence strategies, deviation management, amendment workflows, and investigational product accountability—the operational backbone of GCP-compliant trials.
Navigate the critical world of pharmacovigilance: AE vs. SAE classification, SUSAR expedited reporting, timelines that matter, and documentation that protects participants.
Master ALCOA++ principles—Attributable, Legible, Contemporaneous, Original, Accurate—plus source data verification and electronic systems validation requirements.
Explore the E6(R3) data governance framework—lifecycle management, computerized systems validation, audit trails, and safeguarding trial blinding in the digital age.
Embrace the E6(R3) quality revolution: Risk-Based Quality Management (RBQM), Quality by Design (QbD), Critical to Quality factors, and modern centralized monitoring approaches.
Complete your training with TMF organization, essential document requirements, noncompliance handling, and proven strategies for successful regulatory inspections.
Every clinical trial hinges on a shared language of ethics, documentation, and oversight. The most recent ICH E6(R3) revision raises the bar—demanding smarter risk management, verified digital systems, and human-centred consent workflows.
FreeGCP was built as an open-access reference implementation of those expectations. We blend the rigour of regulatory source documents with annotated case studies and interactive exercises that translate policy into instinct.
The result: a credible credential for individuals and a scalable baseline for organizations who refuse to cut corners on participant safety or data integrity.
Clinical research professionals
CRAs, CRCs, data managers, site coordinators, and quality specialists who need proof of current GCP mastery.
Principal investigators & clinicians
Physicians, pharmacists, and allied health professionals entering or refreshing regulated research work.
Sponsor & CRO leadership
Regulatory, QA, and project leads who must maintain current GCP certification and compliance standards.
Create your free account to access the complete ICH E6(R3) curriculum, knowledge assessments, and professional certificate.
We re-engineered the ICH E6(R3) curriculum into an immersive learning experience: interactive modules, annotated guidelines, and real-world scenarios that mirror the realities of sponsor oversight. No paywalls, no watered-down summaries—just the training you actually need to step into a regulated role.
Credential
ICH E6(R3) Certificate
Issued instantly with QR verification and ledger logging.
Format
Interactive • Case studies • Quizzes
Designed for desktop deep work and mobile refreshers.
Self-paced comprehensive training
Interactive modules, annotated readings, and real-world scenarios crafted by senior CRAs.
Structured assessments
Lesson knowledge checks, module quizzes, and a comprehensive final exam aligned with sponsor expectations.
Instant industry credential
Receive a verifiable certificate with QR validation and ledger ID the moment you pass.
Community
Early feedback from the clinical research community
This will be a great asset to the clinical research community. The ICH E6(R3) focus and comprehensive curriculum coverage is exactly what we need for current GCP training standards.
Clinical Research Professional
Research Community Feedback
All certificates include QR codes and unique IDs for instant verification during audits and inspections.
Explore related topics to deepen your understanding
Begin the FreeGCP track now and earn your verifiable certification. Join coordinators, monitors, and investigators advancing their careers with ICH E6(R3) training.
Create your account in under a minute