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Not all research is subject to clinical trials regulations, but the same standards of conduct apply.
This course in good research practice covers the legislation that applies to ‘non-CTIMP’ research,(e.g. research not involving a clinical trial of an investigational medicinal product) along with the detailed principles of good practice in clinical research studies. This four-hour course comprises didactic teaching, woven into interactive exercises and videos of those experienced in the conduct of clinical research.
* An introduction to GRP * Legislation * Protocol and associated documents * Documentation and study files * Applications, approvals and amendments * Confidentiality * Consent and conducting the study * Web resources
