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...
Good Manufacturing Practice: Annex 13 (Polish)
4.7
★★★★★
97% Recommended
3 hours
120 active users
3 points
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Good Manufacturing Practice: Annex 13 (Polish)
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About
This course provides grounding in the principles of Good Manufacturing Practice – specifically related to manufacturing Investigational Medicinal Products (Annex 13). Applying GMP to IMPs provides assurance that the results of clinical trials are not compromised by inadequate safety, quality or efficacy arising from unsatisfactory product manufacture. It has many other benefits, including ensuring results are comparable across different batches of Investigational Medicinal Products. For the process to work, personnel must have adequate training in requirements specific to Investigational Medicinal Products.
This course is designed for those working with IMPs in clinical trials, offering an interactive and visually appealing format. It provides valuable insights into GMP applications based on the author's professional experience and allows participants to earn 3 CPD points.
Course Benefits
Fully compliant
This course follows the guidance of Annex 13 of the European Commission's GMP guidelines
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 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. Our reporting tools make it easy for administrators to check the progress of learners and identify areas for future training.
Reliable and trustworthy
This course was written by McCarthy Consultant Services Inc (Canadian specialists in regulatory work to support the global pharmaceutical, biotechnology, medical device, food, natural health products and cosmetic industries). You will also stay up to date with any legislative changes in GMP relating to IMPs as our training courses are constantly monitored, reviewed and updated.
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