Module 0140m
GCP Foundations and Principles
Overview of ICH GCP, scope, stakeholders, and core principles including ethics and participant protection.
- GCP overview and scope
- 42 principles of ICH GCP E6(R3)
FreeGCP distills ICH E6(R3) into immersive modules, real-world protocol scenarios, and graded assessments. Earn a certificate respected by sponsors, CROs, and IRBs—completely free of charge.
Enroll in minutes
Create your account—no credit card required.
Master ICH E6(R3)
Interactive modules written by clinical research experts.
Earn proof instantly
Download a verifiable certificate the moment you finish.
Rated 4.9/5 by 12,487 research professionals and study coordinators.
FreeGCP meets the highest regulatory standards. We collaborate with sponsors, sites, and institutional review boards to keep our curriculum provably compliant—and keep access free for every learner.
Regulatory grade
FDA · EMA · MHRA
120+ countries
Learners worldwide
Finish in hours
Self-paced learning
Certified professionals
12,487
Clinical research staff who completed FreeGCP since launch.
Organizations
500+
Sponsors, CROs, and hospitals who rely on our training.
Learner rating
4.9/5
Based on verified reviews from the clinical research community.
Cost to certify
0$
We keep the entire GCP curriculum free—no credit card prompts.
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 commitment
6 hours
Self-paced with progress saved automatically.
Assessments
100+ questions
Scenario-based, aligned with sponsor and site expectations.
Built with senior CRAs, quality leads, and principal investigators.
Overview of ICH GCP, scope, stakeholders, and core principles including ethics and participant protection.
Investigator/site duties, sponsor/CRO obligations, and IRB/IEC oversight per E6(R3).
Process, documentation, and considerations for vulnerable populations under E6(R3).
Protocol adherence, deviations/amendments, and investigational product accountability.
AE/SAE/SUSAR definitions, reporting timelines, and medical care documentation.
Source data, CRF/eCRF, ALCOA++ principles, and electronic systems validation.
Governance of the full data lifecycle, safeguarding blinding, and computerized systems.
QMS, risk assessment, Quality by Design, centralized/onsite monitoring, and CAPA.
TMF organization, essential documents, noncompliance handling, and inspection readiness.
Interactive cases that explore protocol deviations, safety alerts, and complex monitoring challenges.
Verifiable PDF credentials with unique IDs, accessible for audits and HR systems.
Training aligned with ICH E6(R3) standards, meeting FDA, EMA, and MHRA expectations.
Industry-recognized certificate accepted by sponsors, CROs, and institutional review boards.
Knowledge checks after lessons, module quizzes, and a comprehensive final exam to validate understanding.
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.
Who we train
Clinical research teams
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 evidence training across distributed teams and vendors.
Create your free account to access the full curriculum, knowledge checks, and certificate download instantly. Team managers can invite colleagues and monitor completions from day one.
No credit card • Verified certificate • Progress saves automatically
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
Download a verifiable certificate with QR validation and ledger ID the moment you pass.
See what professionals are saying about our training
This platform transformed how our team approaches GCP training. The content is comprehensive, up-to-date, and incredibly easy to digest.
Dr. Sarah Chen
Clinical Research Director at Pfizer
I passed my certification exam on the first try thanks to FreeGCP. The practice questions and real-world scenarios were invaluable.
Michael Rodriguez
CRA II at Novartis
The best online GCP training I've found. Clear explanations, great examples, and excellent support when I needed it.
Emily Thompson
Quality Assurance Manager at Johnson & Johnson
FAQs
If you need program documentation for an inspection or organization-wide rollout, reach out—we can provide signed attestations and completion exports.
Begin the FreeGCP track now and certify faster than traditional classroom programs. Join coordinators, monitors, and investigators across 120+ countries.
Create your account in under a minute · Certificate issued instantly
FreeGCP distills ICH E6(R3) into immersive modules, real-world protocol scenarios, and graded assessments. Earn a certificate respected by sponsors, CROs, and IRBs—completely free of charge.
Enroll in minutes
Create your account—no credit card required.
Master ICH E6(R3)
Interactive modules written by clinical research experts.
Earn proof instantly
Download a verifiable certificate the moment you finish.
Rated 4.9/5 by 12,487 research professionals and study coordinators.
FreeGCP meets the highest regulatory standards. We collaborate with sponsors, sites, and institutional review boards to keep our curriculum provably compliant—and keep access free for every learner.
Regulatory grade
FDA · EMA · MHRA
120+ countries
Learners worldwide
Finish in hours
Self-paced learning
Certified professionals
12,487
Clinical research staff who completed FreeGCP since launch.
Organizations
500+
Sponsors, CROs, and hospitals who rely on our training.
Learner rating
4.9/5
Based on verified reviews from the clinical research community.
Cost to certify
0$
We keep the entire GCP curriculum free—no credit card prompts.
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 commitment
6 hours
Self-paced with progress saved automatically.
Assessments
100+ questions
Scenario-based, aligned with sponsor and site expectations.
Built with senior CRAs, quality leads, and principal investigators.
Overview of ICH GCP, scope, stakeholders, and core principles including ethics and participant protection.
Investigator/site duties, sponsor/CRO obligations, and IRB/IEC oversight per E6(R3).
Process, documentation, and considerations for vulnerable populations under E6(R3).
Protocol adherence, deviations/amendments, and investigational product accountability.
AE/SAE/SUSAR definitions, reporting timelines, and medical care documentation.
Source data, CRF/eCRF, ALCOA++ principles, and electronic systems validation.
Governance of the full data lifecycle, safeguarding blinding, and computerized systems.
QMS, risk assessment, Quality by Design, centralized/onsite monitoring, and CAPA.
TMF organization, essential documents, noncompliance handling, and inspection readiness.
Interactive cases that explore protocol deviations, safety alerts, and complex monitoring challenges.
Verifiable PDF credentials with unique IDs, accessible for audits and HR systems.
Training aligned with ICH E6(R3) standards, meeting FDA, EMA, and MHRA expectations.
Industry-recognized certificate accepted by sponsors, CROs, and institutional review boards.
Knowledge checks after lessons, module quizzes, and a comprehensive final exam to validate understanding.
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.
Who we train
Clinical research teams
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 evidence training across distributed teams and vendors.
Create your free account to access the full curriculum, knowledge checks, and certificate download instantly. Team managers can invite colleagues and monitor completions from day one.
No credit card • Verified certificate • Progress saves automatically
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
Download a verifiable certificate with QR validation and ledger ID the moment you pass.
See what professionals are saying about our training
This platform transformed how our team approaches GCP training. The content is comprehensive, up-to-date, and incredibly easy to digest.
Dr. Sarah Chen
Clinical Research Director at Pfizer
I passed my certification exam on the first try thanks to FreeGCP. The practice questions and real-world scenarios were invaluable.
Michael Rodriguez
CRA II at Novartis
The best online GCP training I've found. Clear explanations, great examples, and excellent support when I needed it.
Emily Thompson
Quality Assurance Manager at Johnson & Johnson
FAQs
If you need program documentation for an inspection or organization-wide rollout, reach out—we can provide signed attestations and completion exports.
Begin the FreeGCP track now and certify faster than traditional classroom programs. Join coordinators, monitors, and investigators across 120+ countries.
Create your account in under a minute · Certificate issued instantly