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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...
GMP & Quality Assurance Learning Path
4.7
★★★★★
97% Recommended
Updated 2025
18 hours
0 active users
18 points
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Each course includes:
Fully compliant
This learning path is aligned with ICH GCP E6 (R3), EU GMP, PIC/S GMP Guide, and FDA cGMP requirements — providing comprehensive compliance coverage for the topics covered. Learners receive Continuing Professional Development (CPD) Points awarded by the Faculty of Pharmaceutical Medicine of the Royal College of Physicians of the United Kingdom.
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 a database, re-sitting the exam does not 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 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 GMP & Quality Assurance Learning Path builds a strong operational foundation in Good Manufacturing Practice and GxP quality systems for professionals working across pharmaceutical, biotech, and manufacturing environments. It covers the core principles of GMP, deviation management and CAPA, internal auditing, and cross-GxP inspection readiness.
Participants will develop the practical knowledge to apply GMP principles day-to-day, investigate deviations effectively, conduct internal audits, and prepare confidently for regulatory inspections across GxP domains.
Courses Included
Core GMP principles, quality culture, and the regulatory framework underpinning pharmaceutical manufacturing.
3 hours
2 pointsA practical, memorable grounding in the ten fundamental GMP rules every operator and quality professional should apply.
3 hours2 points
Structured approaches to deviation handling, root cause analysis, and effective corrective and preventive actions.
3 hours3 pointsPlanning, conducting, and reporting internal GMP audits to identify gaps before external inspections do.
3 hours2 pointsPIC/S GMP expectations and practical steps to ensure ongoing inspection readiness.
3 hours2 pointsCross-GxP inspection preparation, covering common regulator expectations across GMP, GCP, and GVP domains.
3 hours3 pointsOur Certified Customers
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Frequently Asked Questions
- Quality Assurance and Quality Control professionals in pharmaceutical manufacturing
- Manufacturing and production staff seeking GMP grounding
- Internal auditors and inspection-readiness leads
- QA managers preparing sites for regulatory inspection
- Professionals new to GxP quality systems
Upon completion of this learning path, participants will be able to apply core GMP principles, manage deviations and CAPAs effectively, conduct internal GMP audits, and support inspection readiness across GxP domains in line with PIC/S, EU GMP, and FDA cGMP expectations.
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