Cost: To be negotiated
These courses include training in important aspects and best practices of clinical research that are not necessarily covered by GCP guidance alone. The courses can be customized to any level of staff e.g. basic entry-level for lay field workers, intermediate level for study coordinators or research nurses, or advanced for PIs or sub-Investigators.
If your site has a particular need or gap CREDE can tailor make a course to fit your needs.
Some examples of these courses:
- Good documentation practice (GDP): training in designing, completing and quality control of study documentation such as source documents and CRFs
- Clinical Quality control procedures e.g. systems for checking that study procedures , documentation and core study functions are of a high standard
- Informed consent: in-depth training in taking informed consent including special circumstances such illiterate participants, language disparities and translators, underage participants etc.