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The most important areas of regulations and guidelines controlling clinical trials will be covered including: understanding the importance of the EU Clinical Trial Directive; clinical trial authorisations; the increasingly important requirements for running trials in children; requirements for managing investigational medicinal product; legal aspects of clinical trials; pharmacovigilance; data management, GCP requirements; regulatory inspection and more. Topics will also include an update on the latest CT Directive guidelines and other EU Clinical Trial developments.
Related Journals of Regulatory affairs for clinical trails
Clinical Research and Regulatory Affairs, Applied Clinical Research, Clinical Trials and Regulatory Affairs, International Journal of Drug Regulatory Affairs, Applied Clinical Research, Clinical Research and Regulatory Affairs