3 PM - 4 PM
IRB Education Session
DHMC, Borwell 758W
11 AM - 1 PM
GSMD Registrar's Suite, DHMC
This document generally describes Dartmouth's Human Research Protection Program (HRPP) operations, based on human subjects protections regulations and guidance. We invite your comments and questions.
Dartmouth Investigator Transfer Guidelines (from Dartmouth to another Institution)
All items on this checklist should be reviewed and completed PRIOR to departing Dartmouth.
Data Safety Monitoring and Reporting of Adverse Events to CPHS For Clinical Trials
This memo is an update to the requirements for reporting Adverse Events to the CPHS, and also clarifies the importance of rigorous data and safety monitoring in clinical trials involving human subjects.
Classroom Activities and Independent Student Projects
This memo clarifies institutional procedures related to CPHS review of student projects.
Projects specifically recruit Geisel medical school students as potential subjects because of their student status must be reviewed by the Medical Education Institutional Review Committee (MEIRC), as detailed in this memo. Please contact Greg Ogrinc MD for more information.
Last Updated: 11/29/16