October 28, 2020 -
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. This program is strongly encouraged for new investigators and coordinators as they start their clinical research careers as well as those with research experience.
Topics to be discussed include: Federal Regulations Governing Human Subject Research, Protocol Development, Tips for Protocol Adherence, Investigator Responsibilities, Informed Consent and Waivers of Consent, Study Documentation, and Regulatory File Maintenance.
Register here if you are interested in attending the program. Submit advance questions or comments to email@example.com.
Location and Address
This is a virtual event. The link will be sent out prior to the event.