This one-day course takes place on October 19th, 2011 and includes topics designed to appeal to a wide variety of individuals. The afternoon will include several workshops, with several options available in each time slot.
Who should attend?
This course will be of benefit to physician investigators, research coordinators and assistants, as well as those thinking of a career in clinical research.
Course Objectives
The course provides participants with an opportunity to orient themselves to basic and intermediate concepts, theories, definitions, practices, and approaches that apply to clinical research including (but not limited to) gaining awareness of regulations governing clinical research in Canada and privacy.
The interactive Workshop portions of the course will expose participants to more specialized clinical research concepts including trial design, monitoring, systematic reviews, file management, and continuing consent. New this year: French-language workshops in some time slots.
During, and following this course, participants will be able to:
- Apply basic to intermediate clinical research concepts and processes such as understanding which regulations apply to their research, including Health Canada regulations.
- Employ best practices in areas including ethics, privacy, monitoring, and regulatory file management.
- Comprehend and apply specialized and advanced areas of clinical research such as trial design, systematic reviews and risk of bias, and database research.
Attendees will receive a certificate and CME credits for attending.
For more information, please contact:Robert Wouda
rwouda@ohri.ca
613-798-5555 ext 19628
