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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...
GXP Bundle
4.6
★★★★★
91% Recommended
Updated 2025
28 hours
109 active users
28 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.
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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.
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About
The GxP Compliance Bundle is a comprehensive learning program designed to provide a holistic understanding of Good Practice (GxP) requirements across the pharmaceutical, biotechnology, clinical research, laboratory, and distribution environments. This bundle integrates the critical GxP domains that collectively ensure patient safety, data integrity, product quality, and regulatory compliance throughout the product lifecycle.
Covering clinical trials, laboratories, manufacturing, distribution, and investigational product management, the bundle aligns with global regulatory expectations and inspection standards. It is ideal for organizations seeking cross-functional GxP training as well as professionals who need a complete compliance foundation to work effectively in regulated life sciences environments.
Who Should Enrol?
- Entrepreneurs planning to start a medical or pharmaceutical delivery business.
- Logistics and courier professionals expanding services into healthcare distribution.
- Operations managers, warehouse supervisors, and delivery personnel handling pharmaceutical or medical products.
- Quality assurance, compliance, and audit professionals responsible for maintaining regulatory standards in healthcare logistics.
What you will learn
Understand the principles of compliant pharmaceutical and medical product distribution, including GDP/GMP requirements and healthcare logistics standards.
Learn how to establish and manage efficient delivery operations for medicines, vaccines, and clinical supplies while maintaining product quality and patient safety.
Develop skills in implementing quality management systems, compliance processes, staff training programs, and audit readiness practices.
Gain practical knowledge of healthcare logistics operations, warehouse management, risk control, and regulatory expectations for medical product transportation.
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
Focuses on quality and compliance requirements for laboratories supporting clinical trials, ensuring reliable, accurate, and traceable data
6 hours6 points
Provides detailed guidance on the manufacture, packaging, labeling, and handling of Investigational Medicinal Products (IMPs) in compliance with EU GMP Annex 13
3 hours3 pointsCovers regulatory requirements for non-clinical laboratory studies, ensuring study integrity, reproducibility, and inspection readiness
6 hours6 points
Addresses regulatory expectations for the storage, transportation, and distribution of pharmaceutical products to maintain quality throughout the supply chain
7 hours7 pointsOur Certified Customers
Learner Rating & Reviews
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Average Rating
536 global ratings
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Frequently Asked Questions
- Entrepreneurs starting a medical or pharmaceutical delivery company
- Logistics and courier companies expanding into healthcare delivery
- Operations managers and warehouse supervisors
- Delivery drivers handling medicines, vaccines, or clinical supplies
- Quality, compliance, and audit professionals in healthcare logistics
On completion, learners will be equipped to establish compliant delivery operations, train staff effectively, implement quality systems, and meet GDP/GMP expectations for pharmaceutical and medical product distribution.
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