Welcome to GCP on-line!
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This ICH GCP course will give you a current and comprehensive guide to the requirements, conduct and principles of Good Clinical Practice. Packed with information, links, case studies and useful tips, the course is written around the ICH GCP protocols and is fully in line with FDA requirements and regulations.
The course is ideal for health workers who are new to clinical trials and will also provide a timely update for those more experienced. The skills and knowledge learnt are applicable in the US, as well as in clinical trials conducted globally under ICH standards.
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The course has been expertly written by Dr. Laura Brown, currently the Course Director, MSc Clinical Research, Cardiff University, UK. She has 20 years of experience in the pharma industry, pharma training and extensive academic background (PhD, MBA, BSc Biochemistry, BSc Psychology, Post-graduate Diploma in Clinical Sciences). She has also authored and co-authored of 8 books in total, including Learning and Development (2003).
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Certification
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If you score more than 80% on the optional 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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Topics of the GCP course:
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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
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The Principles of ICH GCP
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Informed Consent
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Ethics - IRB Review Boards
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Responsibilities of the Investigator
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Responsibilities of the 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 prerequisite for anyone carrying out, or involved in, clinical research and clinical trials. The course is therefore relevant to:
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Investigators from 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 in approving and monitoring clinical trials
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Members of ethics committees
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Graduates looking to develop a career in clinical research
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| News |
GCP Training in Spanish
10/28/2009
| Infonetica Ltd. has added a new web-based solution relevant to the rising standards and demands... |
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