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...
Laboratory Quality & GLP/GDP Compliance Learning Path
4.7
★★★★★
97% Recommended
Updated 2025
18 hours
195 active users
18 points
If you'd like to swap a course or add additional courses, Customize Your Bundle — or reach out to us and we'll tailor a learning path to your training needs.
Your Study Basket
1 x Laboratory Quality & GLP/GDP Compliance Learning Path
| Total | |
VAT is levied as per your country’s applicable rules and rates at checkout
Each course includes:
Fully compliant
This learning path is aligned with FDA 21 CFR Part 58 GLP, OECD GLP principles, and ISO/IEC 17025:2017 — 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.
Secure Payment Service
Rest assured we use secure processes to protect your payment.
Secured by:
About
The Laboratory Quality & GLP/GDP Compliance Learning Path equips laboratory and quality professionals with the knowledge to operate compliant nonclinical and clinical laboratories. It covers Good Laboratory Practice, Good Clinical Laboratory Practice, ISO/IEC 17025 laboratory management systems, laboratory safety, and biological sample handling.
Participants will develop the skills to maintain laboratory compliance, manage laboratory safety, and handle human biological samples appropriately.
Courses Included
FDA GLP requirements for nonclinical laboratory studies supporting regulatory submissions.
3 hours
2 points
Core Good Laboratory Practice principles applicable across nonclinical research laboratories.
6 hours6 points
Quality principles specific to clinical laboratories supporting clinical trial sample analysis.
6 hours6 points
Implementing and maintaining a laboratory management system in line with ISO/IEC 17025:2017.
2 hours3 pointsLaboratory safety practices and OSHA requirements for protecting laboratory personnel.
3 hours2 pointsProper handling, storage, and transport of human biological samples in research and clinical settings.
2 hours3 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
- Laboratory managers and analysts in nonclinical and clinical laboratories
- Quality professionals responsible for laboratory compliance
- Laboratory safety officers
- Professionals handling human biological samples
Upon completion of this learning path, participants will be able to apply GLP and Good Clinical Laboratory Practice principles, implement an ISO/IEC 17025:2017 laboratory management system, maintain laboratory safety in line with OSHA requirements, and handle human biological samples appropriately.
Best Seller
