-What are the basic HHS regulations and NIH policies that apply to research involving human subjects, including clinical trials?
-How do you prepare a research proposal for review that addresses the regulatory requirements?
-What are some strategies for developing realistic and scientifically acceptable inclusion plans?
Join experts from the NIH Division of Human Subjects Research and HHS Office of Human Research Protections (OHRP) for answers to these questions and additional valuable information and resources. During this 2-day event, these NIH and HHS experts will share policies, resources, guidance, and case studies in this informative and engaging, live event.
For more information about the event, please click here.