Welcome to GCP on-line!
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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 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 basic principles of ICH Good Clinical Practice,
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as well as MHRA regulations. It covers all the changes/amendments proposed in the EU Directive 2005/28/EC and the current UK Regulations. 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.
As part of its multi-language solutions (portfolio page), Infonetica provides online GCP training also in German, Spanish, Italian, Russian and Polish).
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Certification
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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.
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GCP course topics:
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The topics presented in the online GCP training cover all the different aspects of the Good Clinical Practice. Please press the button below to review the training freely.
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Introduction & The Principles of ICH GCP
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Informed Consent
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Ethics
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Responsibilities of Investigator
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Responsibilities of Sponsor
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Clinical Trial Protocol
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Investigator Brochure
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Essential Documents
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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:
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Investigators from NHS organisations, university hospitals, pharmaceutical companies and research institutes
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Clinical trials support staff (e.g staff working in contract research organisations)
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Research Nurses
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R&D staff involved with approving and monitoring clinical trials
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Members of ethics committees
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Clinical trials support staff (e.g CRO staff)
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| News |
GCP Training in Spanish
28/10/2009
| Infonetica Ltd. has added a new web-based solution relevant to the rising standards and demands... |
more
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