Developed by The QARP Academy | Accredited for CPD Points
GCP Auditor School
Fully Remote Clinical Research Auditing Certification Program | Next cohort: September 15, 2026 | April 2026 cohort closed
The GCP Auditor School is an advanced fully remote international program focused on practical auditor training in Good Clinical Practice (GCP).
It provides the competence and certification required for roles in quality oversight, compliance, and audit management across clinical research.
It provides the competence and certification required for roles in quality oversight, compliance, and audit management across clinical research.
The GCP Auditor School offers two learning formats based on the same program structure.
The Full Certification Program provides a complete 10-week training that includes all ten modules, live expert sessions, and a final certification exam leading to the Certified GCP Auditor qualification (CPD Points: 160).
The Modular Learning Track allows participants to choose individual modules according to their professional interests and create a personalized learning path.
Both formats are developed and delivered by The QARP Academy.
The Modular Learning Track allows participants to choose individual modules according to their professional interests and create a personalized learning path.
Both formats are developed and delivered by The QARP Academy.
Full Certification Program
Duration: 10 weeks | Start: September 15, 2026 | CPD Points: 160 | Price: €250/month or €2,000/year
Modular Learning Track
Duration: Flexible | Format: 1-week modules (self-paced)
Study time: 3 hours live + 9 hours self-paced per module.
CPD points per module: 20
Study time: 3 hours live + 9 hours self-paced per module.
CPD points per module: 20
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Certification:
Certified GCP Auditor (CPD UK)
Issued by The QARP Academy, accredited for CPD Points (UK)
Issued by The QARP Academy, accredited for CPD Points (UK)
- Full 10-week program with live expert sessions and final exam
- Recognized international qualification in GCP auditing
- Conducted 100% online via The QARP Learning Platform
PRE-TRAINING ACCESS
An optional preparation track available to participants who register before the official start of the Auditor School.
Pre-training provides a clear way to use the months before the program begins to strengthen core regulatory and technical skills. This format is independent from the main curriculum and does not influence admission or progression within the Auditor School.
All pre-training courses and materials are included in the program fee
Participants who register early receive access to two full professional courses: the advanced ICH GCP E6(R3) program and the Computerized Systems Validation (CSV) program. Access is activated within three business days after payment and remains available until the end of the Auditor School.
Registration date does not limit availability. Participants who join later also receive full access and may complete the materials before the start of the program or in parallel with the main curriculum.
The preparatory track is optional and does not affect requirements or progression in the core program starting in April 2026.
It is designed for specialists who want to strengthen their regulatory and technical foundation in advance and establish a structured path toward the auditor role.
The preparatory track is optional and does not affect requirements or progression in the core program starting in April 2026.
It is designed for specialists who want to strengthen their regulatory and technical foundation in advance and establish a structured path toward the auditor role.
What You Gain After Completing the Program
What You Gain After Completing the Program
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Professional AdvancementGCP auditors and quality specialists play key roles in ensuring compliance of clinical research with international standards.
The program prepares you for high-responsibility positions in pharmaceutical companies, CROs, and research institutions. -
International CertificationGraduates who complete all ten modules and pass the final exam receive the title Certified GCP Auditor (CPD UK) — a qualification recognized in Europe and internationally. -
Career FlexibilityThe acquired skills open access to quality departments, internal and external audit teams, and GxP compliance projects — nationally and globally. -
Practical CompetenceYou will learn not only to assess documentation but to make professional decisions in real audit scenarios, strengthening your expertise and professional standing.
Designed for professionals with at least one year of experience in clinical research or GxP environments:
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- Clinical Research Associates (CRAs)
- QA and Quality Specialists
- Clinical Trial Managers and Leads
- Data Managers and Project Managers
- Regulatory Affairs and Compliance staff
The April 2026 cohort is now closed. The next cohort starts on September 15, 2026 (limited to 30 participants). Pre-training materials are available from the day of purchase. Subscribe now at theqarpacademy.pro — monthly subscription (€250/month) or annual payment (€2,000/year) including all modules, webinars, and certification.
Enrollment countdown — September 2026 cohort:
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Enrollment open — Next cohort: September 15, 2026 | Subscribe at theqarpacademy.pro
Reserve Your Seat — Deposit for September 2026 Cohort
Pay €500 deposit to reserve your place in the September 2026 cohort. Total program fee: €2,000. You can also subscribe directly at theqarpacademy.pro — €250/month or €2,000/year. Pre-training materials are available from the day of purchase. Places are limited to 30 participants.
Full Payment
Pay the full €2,000 tuition fee and secure your place in the September 2026 cohort.
Includes all 10 modules, live expert sessions, course materials, final exam, and CPD-accredited certificate.
You can also subscribe at theqarpacademy.pro — €250/month or €2,000/year. Pre-training materials are available from the day of purchase.
Includes all 10 modules, live expert sessions, course materials, final exam, and CPD-accredited certificate.
You can also subscribe at theqarpacademy.pro — €250/month or €2,000/year. Pre-training materials are available from the day of purchase.
Our team and teachers
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- Dr Maxim BunimovichMD, MRQA, SQA – Founder & Scientific Director, The QARP Academy (Barcelona, Spain)19 years in pharma, 13 years in QA. Led >900 audits and delivered >1,400 training sessions; specialises in site, TMF and CRO audits and in AI‑enhanced learning.
- Dr Stanislav PraslovMD, RQAP‑GCP, MRQA – Senior Auditor & Quality‑Systems Adviser (Mannheim, Germany)20 years’ clinical‑research experience, including 7 years of international GCP auditing and QMS development. Advises on complex GCP issues, vendor selection and CRO oversight.
- Suheila Abdul-KarrimBSc, CCRA, FACRP, RQAP‑GCP – Independent Auditor & Trainer (Johannesburg, South Africa)27 years in clinical‑trial QA, auditing and training. CCRA‑certified since 2000 and member of the ACRP Board, Content Advisory Working Group and Fellows Panel
- Heather ArmstrongBSc – Senior Quality Assurance Auditor (San Diego, USA)23 years in Clinical Trials, GCP and GLP Quality Assurance Director, Consultant supporting multi‑regional clinical trials and inspection‑readiness programmes.
- Retha BritzM.Phil (Medical Law & Ethics), MSc – Clinical Research Quality & Ethics Specialist (Johannesburg, South Africa)19 years in Audits, Consulting and Training, M.Phil in Medical Law & Ethics, Applied Ethics, M.Sc in Physiology. Author of Clinical Research Conduct in South Africa: Informed Consent and first‑author contributor to the South African Medical Journal.
- Dr Denis SyebovMD – Global GxP Quality‑Assurance Consultant (Tbilisi, Georgia)25 years in clinical research; trained in internal medicine and oncology. Conducted ~300 GxP audits worldwide and helped host/lead 115 regulatory inspections (FDA, EMA, MHRA, PMDA).
PRE-TRAINING ACCESS
This structure provides sequential access to materials, enabling consistent development of key competencies throughout the preparatory period without creating pressure or forming barriers for participants who join at a later stage.
Function: establishing the regulatory foundation and defining the individual development trajectory.
Function: strengthening the understanding of regulatory requirements and developing the initial analytical skills expected from an auditor.
Function: building competencies in systems, data integrity, and technical processes relevant to audit practice.
Function: unifying terminology, systematizing core concepts, and forming readiness for program launch.
Most popular questions
Registration is considered complete only when both of the following conditions are met:
- The participant completes an admission interview with The QARP to confirm their suitability for the course.
- The participant finalizes enrollment and payment.
The Certified GCP Auditor (CPD UK) credential is recognized and accepted by U.S.-based QA organizations and employers for internal training documentation. The program is designed to meet international standards, making it applicable globally, including in the U.S. market.
Upon successful completion, participants receive the European Certificate — “Professional Specialization in GCP and GCLP Auditing”.
The program is in the final stage of CPD accreditation; upon completion of the process, participants will be able to receive verified CPD points.
The program is in the final stage of CPD accreditation; upon completion of the process, participants will be able to receive verified CPD points.
Participants study the core materials through self-paced learning on The QARP platform and join a live webinar with an expert once per week for discussion, case analysis, and Q&A.
This format allows for flexible independent study while maintaining direct interaction with industry professionals.
This format allows for flexible independent study while maintaining direct interaction with industry professionals.
The course follows a fixed group schedule to ensure an interactive learning experience and meaningful participation in weekly expert sessions.
While you will retain access to the learning materials for self-review, all assignments, assessments, and the final exam must be completed according to the group timeline.
While you will retain access to the learning materials for self-review, all assignments, assessments, and the final exam must be completed according to the group timeline.
Each group includes 25 participants. This size allows for live interaction, small group work, and personalized feedback from instructors.
The exam consists of:
- An automated theoretical test
- A practical assignment based on an audit report excerpt
- An oral assessment on key course topics
The program includes comprehensive coverage of U.S. regulatory frameworks, such as:
- FDA inspection expectations and practical insights from former FDA inspectors
- Detailed analysis of 21 CFR Parts 50, 56, and 312
Applicants should have at least one year of GCP experience.
Those who do not meet this requirement will be interviewed to confirm their readiness for the program.
Those who do not meet this requirement will be interviewed to confirm their readiness for the program.
Leave a request and we will contact you!
Phone number: +34 625263964
Email: info@theqarp.com
Email: info@theqarp.com
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