If you have already purchased this product and are attempting to access it, please return to the main eLearning page and click on the module you require under the heading 'Current Modules and Access'.
This module allows the learner to get insight into the important requirements of the GCP Directive on the conduct of clinical trials. It also shares the views of various clinical trial personnel on the impact of this Directive on their role.
The module includes information on the UK specific requirements as a result of the incorporation of this Directive into UK law under SI 1928, the module also includes the European view by including the Notice to Applicants, volume 10 on Good Clinical Practice.
This module is aimed at any clinical research personnel involved in the set up, conduct, reporting or archiving of a clinical trial. This module will also provide the standard principles required to satisfy the regulatory requirements and meet the exacting standards of regulatory inspection.
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If you would like to purchase a licence for this or any of our eLearning modules please complete an order form. Prices start from £57.50 including VAT.
Discounts available for NHS and multiple licence purchases.
Please contact the Training and Education Co-ordinator for more information +44(0)1628 53967 elearning@icr-global.org
