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GCP International GCP

Online International GCP Training

Good Clinical Practice Course:

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

An individual can take this course by registering and paying a fee of 61.5 EUR plus VAT. Please note that many organizations have group accounts with us, so it could be beneficial to check with the relevant department within your organization, and see if they are already registered with us.
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Welcome to GCP on-line!

 
Welcome to the on-line Good Clinical Practice course designed and developed by Infonetica Ltd and written by Dr Isaac John, Assistant Director of Research and Development, Ashford and St Peters Hospitals, and Honorary Lecturer at the Royal Holloway, University of London. The course is endorsed by Royal Holloway, University of London. The course is also endorsed by the Royal Holloway, University of London and carries 9 CPD (Continuous Professional Development) points.
 
Our course will give you an up-to-date and comprehensive guide to the internationally recognized basic principles of ICH-Good Clinical Practice It covers all the changes/amendments proposed in the EU Directive 2005/28/EC. The Summary of Proposed Changes to current Regulations is attached for ready reference and those changes are also included in all relevant chapters of the course.
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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.
 
Certificate Preview

GCP course topics:

 
  Introduction & The Principles of ICH GCP
  Informed Consent
  Ethics
  Responsibilities of Investigator
  Responsibilities of Sponsor
  Clinical Trial Protocol
  Investigator Brochure
  Essential Documents
View table of contentCourse preview
Useful links & documentsGCP Glossary

Who should take the course?

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As prescribed by the international standards and requirements, a basic understanding of Good Clinical Practice is pre-requisite for anyone carrying out, or involved with, clinical research and clinical trials. The course is therefore relevant to:
 
  Investigators from NHS organisations, university hospitals, pharmaceutical companies and research institutes
  Research Nurses
  R&D staff involved with approving and monitoring clinical trials
  Members of ethics committees
  Clinical trials support staff (e.g CRO staff)
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News
Infonetica Announce the Launch of Tissue Auditor
05/07/2007

Tissue Auditor is designed to meet the new regulatory requirements of handling human tissue samples... more

Infonetica Awarded Tender to Develop UK Integrated Research Governance Form
04/01/2007

Infonetica has been awarded a tender to develop the UK Integrated Research Governance Form.. more

Dendrite announces Infonetica deal to give customers access to an even broader set of NHS data
20/10/2006

Dendrite UK is now able to offer its customers even more comprehensive data on the structure,.. more

 View all news



 
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