New
SM
Clara Fargo
EBMT Clinical Research Quality Assurance Coordinator
I have finalised the demo for the ICH-GCP E6 R3 refresher course. Overall, I liked the content and the interface. I also want to thank Whitehall Train...
Clinical Trials Foundation Path
4.4
★★★★★
94% Recommended
Updated 2025
22 hours
182 active users
22 points
If you'd like to swap a course or add additional courses, simply let us know — Reach out to us and we’ll customize a learning path tailored to your training needs.
Your Study Basket
1 x Clinical Trials Foundation Path
| Total | |
VAT is levied as per your country’s applicable rules and rates at checkout
Each course includes:
Fully compliant
This course meets the required standard for basic GCP training, allowing learners to work on clinical trials. Learners also receive 6 Continuing Professional Development (CPD) Points awarded by the Faculty of Pharmaceutical Medicine of the Royal College of Physicians of the United Kingdom. These can be used to count towards the distance learning element of any scheme that comes under the umbrella of The Academy of Medical Royal Colleges or any other scheme for which there is mutual recognition.
Certified
All learners who pass the final exam receive a uniquely numbered, personal certificate to demonstrate their subject knowledge. Since the questions are picked randomly from database, re-sitting the exam doesn’t mean taking the same questions again and again.
Affordable
Our cost-effective prices represent excellent value. You can easily pay up to ten-times more for face-to-face training. We can also offer generous group discounts on larger purchases.
Time-saving
Our new administration system makes it incredibly quick and simple to allocate licences to multiple learners. Learners save time too by choosing when and where they complete the training.
Secure Payment Service
Rest assured we use secure processes to protect your payment.
Secured by:
About
Build a strong foundation in clinical research through this comprehensive learning path featuring ICH GCP E6(R3), Informed Consent in Clinical Research, Good Documentation Practices and Data Integrity (GDocP), Trial Master File (TMF) Excellence, and CyberSecurity Essentials for Life Sciences & Clinical Research. Designed to provide a practical understanding of clinical trial regulations, ethics, documentation standards, data integrity, inspection readiness, and digital compliance for professionals entering or advancing in clinical research.
Who Should Enrol?
- Clinical Research Associates (CRAs) and clinical research professionals new to the industry.
- Healthcare professionals transitioning into clinical research roles.
- Students and graduates aiming to build a career in clinical trials.
- Clinical Trial Coordinators, site staff, regulatory affairs, quality assurance, sponsor teams, CRO personnel, and clinical operations professionals.
What you will learn
Understand the fundamentals of clinical trials, including study phases, regulatory frameworks, and ethical principles governing clinical research.
Learn essential documentation practices, Trial Master File (TMF) management, and Good Clinical Practice (GCP) requirements for maintaining compliance.
Develop knowledge of data integrity, patient safety principles, and quality systems used in global clinical trial environments.
Gain awareness of cybersecurity principles and regulatory expectations that ensure secure and compliant handling of clinical trial data.
Courses Included
Covers the latest ICH GCP R3 principles, emphasizing quality-by-design, risk-based approaches, and data integrity across clinical trial planning and execution
6 hours
6 points
Learn the ethical and regulatory requirements for obtaining and documenting informed consent in clinical trials.
2 hours3 pointsUnderstand how to maintain accurate, complete, and compliant records to ensure data integrity across regulated processes.
3 hours3 points
Gain practical knowledge on building, managing, and maintaining inspection-ready Trial Master Files throughout the study lifecycle.
2 hours3 points
Explore key cybersecurity principles and best practices to protect sensitive clinical and life sciences data from digital threats.
1 hours2 pointsOur Certified Customers
Learner Rating & Reviews
4.7
★★★★★★
Average Rating
536 global ratings
★★★★★
87.0%
★★★★★
5.0%
★★★★★
3.0%
★★★★★
3.0%
★★★★★
2.0%
Frequently Asked Questions
- Clinical Research Associates (CRAs) Healthcare professionals transitioning into clinical researchStudents and graduates pursuing a career in clinical trials
- Clinical Trial Coordinators and Site Staff
- Clinical Research Professionals new to the industry
- Regulatory Affairs and Quality Assurance professionals
- Sponsors, CRO personnel, and Clinical Operations teams
- Healthcare professionals transitioning into clinical research
Upon completion of this learning path, participants will have a strong foundational understanding of clinical research regulations, ethics, documentation practices, TMF management, data integrity, and cybersecurity principles required to support compliant and high-quality clinical trials.
Best Seller
