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ICH GCP R3 Transition course
€ 99
excl. VAT

Explore the biggest changes in the Good Clinical Practices revision from R2 to R3 and it’s impact on your clinical trial

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Expert ICH GCP Course for Sponsors in International Clinical Trials
€ 99
excl. VAT

Learn everything you need to know to master the Sponsor responsibilities of ICH GCP for International Clinical trials

 

 

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MDR Course for Clinical Research
€ 199
excl. VAT

Learn about the setup and conduct of clinical trials with medical devices in Europe according to the MDR.

 

  • Self-paced online course
  • Written by experts
  • Recognized certificate
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EU CTR Expert
€ 95
excl. VAT

Our all inclusive EU CTR Expert course for clinical drug trials in Europe helps you understand all the vital aspects of the EU CTR regulation.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Master the new EU CTR regulation efficiently.

  • 7,5 hours
  • 4 modules 
  • Online certificate
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Expert ICH GCP Course for Sites in International Clinical Trials
€ 99
excl. VAT

Learn everything you need to know to master the Site's responsibilities of ICH GCP for International Clinical trials.

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Online ICH GCP training
€ 175
excl. VAT

Expert Online ICH GCP Course for International Clinical Trials

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

The ICH/GCP course is the perfect online training for research professionals working on international trials. 

  • case based
  • active learning
  • recognized GCP certificate
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EU CTR Foundation
€ 50
excl. VAT

Learn the fundamental elements of the new EU CTR.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

The EU CTR Foundation course gives you the fundamentals of the new EU CTR regulation.

  • 1,5 hours 
  • 1 Module 
  • online certificate
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Basic CFR course for clinical trials in the USA
€ 65
excl. VAT

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Add this course to the Expert Online ICH GCP Course for International Clinical Trials

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Learn about the principles the Code of Federal Regulations (CFR) add to the ICH-GCP expectations and get a detailed understanding of the knowledge required for clinical trials in the USA.

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Introductory GMP Quality Oversight Course for European Drug Products
€ 99
excl. VAT

Learn about the principles of Good Manufacturing Practice (GMP), the legal requirements and best practices for effective and efficient Quality Oversight on external manufacturing. Consists of 3 interactive module containing 7 chapters.

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The Clinical Study
€ 79
excl. VAT

Basic course on fundamental knowledge in clinical studies

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GCP Refresher (AMG)
€ 199
excl. VAT

Refresher course for study nurses and members of an investigational team in clinical trials according to the German Medicines Act, the AMG

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Update Course Clinical Trial Regulation (EU) Nr. 536/2014
€ 199
excl. VAT

Update course for nurses and members of a trial team in clinical trials under the Medicines Act (AMG) and Regulation (EU) No. 536/2014

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Prerequisites for Drug Trials
€ 199
excl. VAT

Learn about the regulatory-ethical prerequisites for the conduct of clinical drug trials

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EU CTR Conduct
€ 65
excl. VAT

Our EU CTR Conduct e-learning course gives you the essentials on the upcoming EU CTR regulation, as well as an in-depth understanding

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