Accredited and Trusted Advanced GPC Certification for All Levels, Utilized by Top Executives and Transitioning Alumni Who Are Now Leading Voices. 100% Money-back Guarantee with 14 Day Refund Policy. Payment Plans Available.
($500 Value) 70 In-Depth Advanced GCP Training Modules + E6(R3) Immersive Training Modules + GCPC Study Guide + Certification Exam Backed by CPD + CME Credits. Lifetime Access to Unmatched Curriculum.
2025 Good Clinical Practice Online Course Syllabus
Good Clinical Practice Training Overview
21-Day GCP Career Accelerator Plan
GCP Career Templates (Resume, LinkedIn, Email)
Live Review Webinar -
An Introduction to Clinical Research
FREE PREVIEWFoundations of Clinical Research
Evolution of Ethics in Clinical Research
An Overview of ICH GCP
Phases of Clinical Trials
Regulatory Foundations: Code of Federal Regulations
CFR 21 Part 11
CFR 21 Part 11 Compliance
Code of Federal Regulations
The Role of Regulatory Authorities in Clinical Trials (ICH GCP)
International Clinical Trial Harmonization
Investigational Product (IP) Development Lifecycle
Protocol Development and Application Review
Roles and Responsibilities in Clinical Trial Management (ICH GCP)
Sponsor/CRO Responsibilities
13 Principles, IRB, & Investigator Roles
Informed Consent
Safety of Human Subjects in Clinical Research
Reporting Responsibilities of the Investigators
Adverse Events
Patient Rights and Risk-Benefit Analysis in Clinical Trials
Designing Effective and Accessible Consent Forms
Mitigating Risks in Vulnerable Populations in Clinical Trials
Adverse Event Classification and Reporting
Ethics in Placebo Use and Randomization in Clinical Trials
Data Privacy and Confidentiality in Clinical Trials
Participant Retention Strategies in Clinical Trials
Crisis Management in Clinical Research
Monitoring Data Integrity for Participant Safety in Clinical Trials
Withdrawal Processes and Ethical Concerns in Clinical Trials
The course is effectively designed to be easily understood by the candidates, even the certification examination is designed to be easily accessed.
The course is effectively designed to be easily understood by the candidates, even the certification examination is designed to be easily accessed.
Read LessVery comprehensive and enlightening, definitely recommend to professionals
Very comprehensive and enlightening, definitely recommend to professionals
Read LessLoved the course as a whole.
Loved the course as a whole.
Read LessI enjoyed learning in this course. It was very concise and up-to-date. Thank you.
I enjoyed learning in this course. It was very concise and up-to-date. Thank you.
Read Lessgreat information on requirements and references
great information on requirements and references
Read LessSee Where AGCPC Alumni Work
| AGCPC™ Graduate Results | Details |
|---|---|
| AGCPC Certification Overview | • Online accredited Good Clinical Practice (GCP) certificate issued upon completion • Certification worth 70 CPD hours with scenario-based training and proctored exam • Passing score: 70% (two attempts included) • Blockchain-verifiable certificate, digital URL credential, and LinkedIn badge |
| Graduates Work At | University research groups · Hospitals · Clinics · Clinical trial sites · Pharmaceutical companies · Government agencies including FDA · NHS · ICON PLC · PPD · IQVIA · Parexel · Johnson & Johnson · Medtronic · Novartis · Novo Nordisk · UNC Health · NYU Langone Health · MD Anderson · Colorado State University · Baylor College of Medicine · Kaiser Permanente · Cornell University · Boston University |
| Job Titles Earned After Certification |
Research Roles: Research Assistant · Lab Assistant · Research Coordinator · Research Scholar · Postdoctoral Researcher · Graduate Research Assistant Internship Roles: Research Assistant Intern · Outpatient Pharmacy Intern Clinical Roles: Clinical Affairs Intern · Clinical Fellow · Clinical Nurse · Clinical Operations Manager · Clinical Research Professional Teaching Roles: Assistant Professor · Lecturer · Graduate Teaching Assistant Management Roles: Clinical Research Manager · Pharmacy Operations Manager · Associate Director of Clinical Development · Vice President of Clinical Development Specialized Roles: Drug Safety Associate · Regulatory Specialist · Scientific Consultant · Medical Laboratory Scientist · Pharmacovigilance Associate Other Roles: NHS Primary Care QI Facilitator · Government Healthcare Recruiter · Research Ethics Coordinator |
View ICH GCP Certification Skills
| Chapter & Lessons | Objectives & GCP Skills |
|---|---|
| Introduction & Career Accelerator: GCP Training Overview; 21‑Day Career Accelerator Plan; GCP Career Templates (Resume, LinkedIn, Email); Live Review Webinar | Navigate course structure and professional development tools; implement GCP career templates for resume, online profile, and outreach; engage in live review sessions. |
| Foundations of Clinical Research & Regulatory Frameworks: An Introduction to Clinical Research; Foundations of Clinical Research; Evolution of Ethics in Clinical Research; Phases of Clinical Trials; Role of Regulatory Authorities; International Harmonization; IP Development Lifecycle; Protocol Development & Application Review; ICH GCP Overview; CFR 21 & Part 11 Compliance | Master foundational research concepts, trial phases, ethics history, and international regulatory harmonization; apply CFR 21 Part 11 electronic‑records compliance; oversee IP lifecycle and protocol design under ICH GCP. |
| Roles & Responsibilities in Trial Management: Sponsor/CRO Responsibilities; 13 GCP Principles (IRB & Investigator Roles); Investigator Responsibilities; Research Nurse & Coordinator Roles; CRA Monitoring Role; Trial Site Staff & Team Responsibilities; Trial Documentation Management; Audit Readiness; Handling Noncompliance & Deviations | Define stakeholder roles and delegation; enforce GCP principles across CRO, IRB, and investigator functions; manage trial documentation and site staff; prepare for audits and resolve protocol deviations. |
| Informed Consent & Patient Safety: Informed Consent (ICH GCP §4.8); Patient Rights & Risk‑Benefit Analysis; Consent Form Design; Vulnerable‐Population Risk Mitigation; Safety of Human Subjects; Crisis Management; Withdrawal Processes & Ethics | Implement GCP‑compliant consent processes; design accessible forms; conduct risk‑benefit assessments; protect vulnerable subjects; manage crisis scenarios and participant withdrawal ethically. |
| Adverse Event Reporting & Responsibilities: Investigator Reporting Responsibilities; Adverse Events; AE Classification & Reporting; Ethics in Placebo Use & Randomization; Data Privacy & Confidentiality; Participant Retention Strategies; Data Integrity Monitoring | Oversee AE and SAE reporting per ICH E2A/E6; classify and report events; ensure data privacy (HIPAA/GDPR); maintain participant retention and data‑integrity monitoring. |
| Ethical Research in Vulnerable Populations: Children; Mentally Incapacitated; Pregnant Women & Fetuses; Prisoners | Apply specialized ethical frameworks and assent/consent requirements for vulnerable groups; ensure additional safeguards in protocol and monitoring. |
| Trial Management, Data Handling & Record Retention: Trial Management Principles; Data Handling & Record Retention; Common Terminology & Abbreviations; Timelines & Milestones; Investigator Site File & Regulatory Binders; EDC Systems; Statistical Principles; Audit Preparation | Manage trial operations including data capture, storage, retention, and audit trails; configure EDC and ISF; apply statistical timelines, milestones, and audit‑preparation best practices. |
| Advanced Trial Management & Risk‑Based Monitoring: Risk‑Based Monitoring Approaches; SDV & Centralized Monitoring; Investigator‑Initiated Trials; Trial Insurance, Budgeting & Contracts; Multisite Trial Management | Design and implement RBM frameworks; perform SDV and centralized monitoring; manage IITs; oversee trial budgeting, insurance, and multisite coordination. |
| Advanced ICH GCP Applications & Future Trends: High‑Risk Trial Compliance; Global Regulatory Harmonization; Multinational GCP Implementation; ICH E6(R3) & E8(R1) Revisions; Digital Health Technologies; Decentralized Models; Adaptive Design Trials; Preparing for 2025+ GCP Compliance | Integrate latest GCP revisions and digital health compliance; adopt decentralized and adaptive trial designs; prepare for evolving global regulatory standards. |
| Certification & Exam: GCP Final Exam Study Guide; ICH GCP Competency Exam (15 Questions) | Validate mastery of GCP principles, regulatory requirements, and practical applications through a competency exam and study guide. |
AGCPC Trains Future Clinical Research Leaders with Unmatched Depth and Interactiveness.
| Provider / Course | Core Offering & Credentials | Price + Renewal & Key Pros / Cons |
|---|---|---|
| CCRPS – AGCPC™ Good Clinical Practice Certification | • 73 multimedia lessons • 20 + hrs HD video • 70 CPD hrs • 300 + quiz Qs • 400 + real-world examples, review tables & full case simulations • 25-Q proctored exam + study guide • CPD-accredited, TransCelerate-recognised • URL-verified PDF & LinkedIn badge • Lifetime access with free biennial refreshers |
$199 (or 4 × $55) Pros: deepest E6 R3 / E8 R1 coverage; weekly live faculty calls; career-accelerator kit; 14-day refund Cons: none at this price / feature mix |
| A: Academic Slide-Based GCP Course | • Slide/quiz modules ≈ 4–6 hrs • TransCelerate-recognised quizzes • Integrates with university/hospital LMS |
≈ $130 per learner Renew every 3 yrs (paid refresher) Pros: widely accepted in academic settings; easy bulk rollout Cons: teaches E6 R2; limited depth; no live support |
| B: Government-Sponsored Free GCP Course | • 12 text-heavy modules ≈ 6 hrs • Quiz ≥ 80 % for printable certificate (valid 3 yrs) |
Free Retake whole course every 3 yrs Pros: zero cost; meets basic federal requirement Cons: no CPD/CE credit; minimal interactivity; no faculty access |
| C: Live Two-Day Virtual GCP Seminar | • Real-time instructor-led class ≈ 15 CE hrs • Pre/post test • Accredited pharmacist CEUs |
$1 600 – 1 900 Annual paid refresher Pros: direct instructor interaction; formal CE credit Cons: high cost; fixed schedule; E6 R2 focus |
| D: Interactive GCP Simulation Module | • Gamified scenario ≈ 2 hrs • Pass/fail; awards 2 continuing-ed credits |
$240 (non-member price) Renew every 3 yrs (paid) Pros: fast, engaging “game” format Cons: very short; no CPD hours; surface-level coverage |
| E: 90-Minute Video Micro-Course | • Video + quiz ≈ 1.5 hrs • Completion certificate only |
$100 – 150 Renew every 3 yrs Pros: quick refresher; trusted IRB provider Cons: E6 R2 content; no CPD; no live faculty |
Learn more about GCP Certification
| Question | Answer |
|---|---|
| 1. What makes our GCP certification different from the basic courses I can watch online? | A credible gcp certification has three hallmarks: it is current (aligned to ICH E6 R3), it is assessed (you pass a proctored, scenario-based exam), and it is recognised by sponsors. AGCPC™ ticks all three boxes and even hashes your certificate to a public blockchain so auditors can confirm authenticity in seconds. Free slide decks and videos are fine for a quick refresher, but they rarely satisfy TransCelerate or FDA BioResearch Monitoring inspectors who want documented, high-stakes assessment. |
| 2. Does this program award an official Good Clinical Practice certification or just a completion badge? | You graduate with an accredited good clinical practice certification worth 70 CPD hours. More importantly, the course embeds mock audits, SAE drills, and consent-form rewrites so you can defend your decisions, not just hang a diploma on the wall. The PDF, online certificate, and LinkedIn badge are simply proof of the competence you build inside the curriculum. |
| 3. Is the GCP training itself interactive, or am I mostly reading slides? | Real gcp training is experiential here. After the monitoring module you draft a site-visit letter; after the 21 CFR Part 11 lesson study on validating an eSource platform. Learning by doing and application beats hour after hour of passive slides and it sticks. |
| 4. How do you keep your good clinical practice training engaging enough that I actually remember it? | Our good clinical practice training blends flash quizzes for every lesson (300+ questions), review tables, case simulations, and more. Alumni say ALCOA+ and “first-patient-first-visit” milestones feel as intuitive as charting vital signs because they’ve rehearsed them in multiple formats. |
| 5. Is there a difference between your course and a generic good clinical practice GCP trainingmodule I saw on YouTube? | Absolutely. In our good clinical practice GCP training regulatory theory meets execution. You don’t just read § 4.5 on investigational-product accountability, you build a working drug-accountability log that you could drop into any TMF tomorrow morning. |
| 6. What deliverables come with the good clinical practice certificate I’ll receive? | Your good clinical practice certificate arrives three ways: a high-resolution PDF for the TMF, a digital certificate with URL, and a LinkedIn badge. |
| 7. My recruiter asked for a recent GCP certificate. How do you define “recent,” and will yours expire? | Most hiring managers define “recent” as within the last two years. Our gcp certificate never technically lapses because you’ll get free renewal micro-modules every second year; finish the 90-minute refresher and a new date-stamped PDF auto-generated, at no extra cost. |
| 8. What should I look for when comparing one GCP course to another? | Any reputable gcp course should publish faculty bios, curriculum-update cadence, and hidden fees right up front. We disclose everything, no surprise charges for exams, renewals, or proctoring. Also examine whether the course already covers E6 R3; many still teach R2. |
| 9. How is your good clinical practice course structured for people with different roles? | The modular good clinical practice course lets pharmacists zero-in on consent and IP handling, while data managers can deep-dive Part 11 and eSource. The final exam, however, still requires holistic integrity, because regulators expect cross-functional awareness. |
| 10. Does the credential count as an ICH GCP certification in the EU and Asia-Pac? | Yes. A modern ich gcp certification must already address ICH E6 R3 annexes, quality-by-design, and critical-data mapping. Our lessons cross-reference EMA, MHRA, PMDA, Health Canada, and Anvisa guidances so you’re fluent everywhere your study runs. |
| 11. I found a site offering a good clinical practice certification free. Why pay $199 here? | A good clinical practice certification free refresher is handy for a surface review, but it rarely includes proctoring, CPD hours, or TransCelerate recognition. If you need documented assessment, verified credentials, and live mentoring, a modest tuition pays career-long dividends, and may save a costly audit finding later. |
| 12. We’re a CRO; can you provide an enterprise-level good clinical practices certificationsolution? | Absolutely. Our enterprise dashboard bulk-enrols staff, tracks quiz scores, and exports certificates—delivering the scalable good clinical practices certification evidence you need to satisfy ICH E6 § 2.8 for investigator qualification. |
| 13. Is there any legitimate way to get a GCP certification free? | “gcp certification free” usually translates to non-assessed slide decks or quizzes without a proctor. Useful for personal learning, yes; but auditors may reject slide-only proof. Investing once in AGCPC™ prevents future corrective-action costs. |
| 14. How does your GCP certification training help with real audit scenarios? | Our gcp certification training turns FDA warning letters into workshops. You’ll draft CAPAs based on genuine 483s, defend them live during office hours, and graduate comfortable under inspection spotlight. |
| 15. What exactly is listed on the GCP training certificate I’ll get? | The gcp training certificate itemises competencies—risk-based monitoring design, SAE narrative drafting, eConsent validation—so managers can map your skills to protocol needs fast. |
| 16. I’m on a tight budget. What’s the true good clinical practice certification cost over five years? | Single tuition is $199 for life. Competing platforms that charge $100 per renewal will cost $500+ in the same period. So the good clinical practice certification cost here ends up the lowest total cost of ownership. |
| 17. Does the program cover new info on AI and DCTs? I need a GCP certification clinical research credential that looks forward. | Yes. Modern gcp certification clinical research includes AI safety-signal detection, decentralized-trial logistics, and wearable data integrity. An entire module addresses these frontiers so your CV remains future-proof. |
| 18. Is there a preview or good clinical practice training free sample before I buy? | Definitely. You can test-drive four lessons of our good clinical practice training free preview, no card required. Get a feel for the platform before you commit. |
| 19. How does your advanced module differ from other ICH GCP training I’ve seen? | Our ich gcp training stitches historical ethics, regional regs, and tech innovation into one story, so you can talk fluently with inspectors about past precedents, current expectations, and future drafts, all in the same conversation. |
| 20. Bottom line: Why should I trust AGCPC™ over dozens of other options? | Because we give you a living, renewable credential, rooted in hands-on skills and prep for higher level roles, that pays for itself the first time you sail through an audit or negotiate a raise. When you're searching for gcp course, good clinical practice certification cost, or ich gcp training and comparing programs, the answer is the same: learners who finish AGCPC™ walk into their next study visit smarter, calmer, and measurably more valuable to their teams. |
Good Clinical Practice Certification
I really enjoyed this training. The content was relayed in a comprehensible manner, making it "easy" to absorb the information. I highly recommend this training to anyone in (or transitioning into) the clinical research industry.
I really enjoyed this training. The content was relayed in a comprehensible manner, making it "easy" to absorb the information. I highly recommend this training to anyone in (or transitioning into) the clinical research industry.
Read LessThe ICH GCP course reinforced my understanding on the APVASC. The material was clearly presented
The ICH GCP course reinforced my understanding on the APVASC. The material was clearly presented
Read LessGood points
Good points
Read LessIt is good course, summarises most of important GCP points and more
It is good course, summarises most of important GCP points and more
Read LessInformative session
Informative session
Read LessI am honestly impressed with the comprehensive coverage of global clinical research standards. The course was well structured, and the material was easy to follow. I highly recommend this certification to anyone involved in clinical research.
I am honestly impressed with the comprehensive coverage of global clinical research standards. The course was well structured, and the material was easy to follow. I highly recommend this certification to anyone involved in clinical research.
Read LessThe material are fluently presented and understandable.
The material are fluently presented and understandable.
Read LessThe course is effectively designed to be easily understood by the candidates, even the certification examination is designed to be easily accessed.
The course is effectively designed to be easily understood by the candidates, even the certification examination is designed to be easily accessed.
Read LessI am Dr Hira Babar, Hematologist by Profession. I took the Advanced Good Clinical Practice Course as well as the quiz at the end of the course. I was an extensive course with a detailed overview of the topics. I thoroughly enjoyed the videos and t...
Read MoreI am Dr Hira Babar, Hematologist by Profession. I took the Advanced Good Clinical Practice Course as well as the quiz at the end of the course. I was an extensive course with a detailed overview of the topics. I thoroughly enjoyed the videos and the slides. I made my own notes of the bullet points. It showed in a very elaborative way how to conduct clinical trials, its stages, the role of coordinator, the challenges and how to report final outcome of the trials. It was an excellent course
Read LessGood points
Good points
Read LessLoved the course as a whole.
Loved the course as a whole.
Read LessLoved the course as a whole.
Loved the course as a whole.
Read LessThe course is effectively designed to be easily understood by the candidates, even the certification examination is designed to be easily accessed.
The course is effectively designed to be easily understood by the candidates, even the certification examination is designed to be easily accessed.
Read LessI am honestly impressed with the comprehensive coverage of global clinical research standards. The course was well structured, and the material was easy to follow. I highly recommend this certification to anyone involved in clinical research.
I am honestly impressed with the comprehensive coverage of global clinical research standards. The course was well structured, and the material was easy to follow. I highly recommend this certification to anyone involved in clinical research.
Read Less