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Online GCP Training

Good Clinical Practice Course


Current and comprehensive guide to the basic
principles of ICH Good Clinical Practice

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Welcome to GCP training online!

Our online courses offer a flexible and cost effective learning opportunity to develop your GCP skills. We offer industry recognised training to add to your professional experience, you can gain professional certification as well as CPD points. Online GCP training means you can study when it suits you!
ICH GCP Course

The course is a current and comprehensive guide to the basic principles of ICH Good Clinical Practice. It reviews and demonstrates the principles of GCP including MHRA regulations and meets the requirements for GCP training as set down in the ICH guidelines.
The course was written by Nick Deaney who has 30 years' experience up to Research Director level in a major pharma group. He is now a professional trainer, giving courses on GCP and clinical research.


Who should take the course?

If you need to brush up on your existing knowledge or are looking for a solution that will enable you to achieve certification in a relatively short time, this course is for you! Those new to clinical research or experienced staff from the NHS, University Hospitals, Pharma, CROs and research institutes will find the course invaluable. As will investigators, clinical trials support staff, research nurses and ethics committee members.
ICH GCP “Interactive” Course

This course is not only a comprehensive guide to ICH-GCP but contains interactive Q&A sessions throughout to help re-inforce the learning process. The questions are structured on the kind of issues you will face in your research career and are based on real life examples encountered by author, Nick Deaney; who has 30 years’ experience up to Research Director level in a major pharma group. This course also meets the requirements for GCP training as set down in the ICH guidelines.

Who should take the course?

If you have the additional time to devote, then the interactive course is the ideal choice – especially if you have relatively little experience at the sharp end of trials work. Those new to clinical research or experienced staff from the NHS, University Hospitals, Pharma, CROs and research institutes will find the course invaluable. As will investigators, clinical trials support staff, research nurses and ethics committee members.
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Added features
  • Meets the ICH guidelines’ requirements for GCP training
  • Available translated into Bulgarian, French, Italian, Japanese, Polish, Portuguese, Russian & Spanish
  • Available in country-specific versions tailored to the individual regulatory requirements of the UK, the US and Germany (in German)
  • Carries 6 CPD points accredited by The Faculty of Pharmaceutical Medicine, London.
Content
  • Chapter 1: Introduction to GCP
  • Chapter 2: Competent Authorities (CA) and Independent Ethics Committee (IEC)
  • Chapter 3: Investigator
  • Chapter 4: Sponsor's Responsibilities
  • Chapter 5: Monitor's Responsibilities
  • Chapter 6: Safety & Adverse Event Reporting
  • Chapter 7: Clinical Trial Protocol and Amendments
  • Chapter 8: Investigator Brochure
  • Chapter 9: Essential Documents
  • Glossary
  • Useful Documents

All our Online GCP Training material includes all the changes/amendments proposed in the EU Directive 2005/28/EC and is in line with current regulations.

All trainees receive full access to the course content, resources and useful documents for 6 months after account activation
Added features
  • Meets the ICH guidelines’ requirements for GCP training
  • Available in an international version or one tailored to the individual regulatory requirements of the UK
  • You can solve problems as you work through the course to reinforce your learning
  • Carries 9 CPD points accredited by The Faculty of Pharmaceutical Medicine, London.

Content
  • Chapter 1: Introduction to GCP
  • Chapter 2: Competent Authorities (CA) and Independent Ethics Committee (IEC)
  • Chapter 3: Investigator
  • Chapter 4: Sponsor's Responsibilities
  • Chapter 5: Monitor's Responsibilities
  • Chapter 6: Safety & Adverse Event Reporting
  • Chapter 7: Clinical Trial Protocol and Amendments
  • Chapter 8: Investigator Brochure
  • Chapter 9: Essential Documents
  • Glossary
  • Useful Documents

All our Online GCP Training material includes all the changes/amendments proposed in the EU Directive 2005/28/EC and is in line with current regulations.

All trainees receive full access to the course content, resources and useful documents for 6 months after account activation
Click Here To Buy Click Here To Buy

Certification

If you score more than 80% on the GCP exam, we will issue you with a certificate for your records and if you agree, your name and organisation details will be added to a database of GCP certified personnel that have passed this course. This database can be publicly accessed.
CLICK HERE FOR CERTIFICATE PREVIEW!
News
New Online Good Clinical Laboratory Practice course launched
1/29/2014
Today, Whitehall Training has launched a new online GCLP course. The course was written by Louise Handy – Chairperson of the Research Quality Association (formerly BARQA – who published the first GCLP guidance). more

Why aren’t medical devices tested like drugs?
1/28/2014
Earlier this week, the BBC Radio Four programme “Face the Facts” highlighted the scandalous state of the medical device sector. Their report centred on some women who had experienced extreme adverse reaction to trans-vaginal mesh implants. The programme went on to complain about the lack of the highly controlled and blinded testing regime undergone by drugs. more

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