Overseeing a research study can be challenging, especially if you are new to the research environment. This workshop will provide an overview of the various components of Good Research Practices. Topics to be discussed include: Federal Regulations Governing Human Subject Research, Tips for Protocol Adherence, Investigator Responsibilities, Informed Consent, Study Documentation, and Regulatory File Maintenance.
This program is strongly encouraged for new investigators and coordinators as they start their clinical research careers as well as those with research experience.
Register is required as seating is limited. Submit advance questions or comments to email@example.com.
Wednesday, June 26 at 9:00 a.m. to 11:00 a.m.