3 PM - 4 PM
IRB Education Session
DHMC, Borwell 758W
11 AM - 1 PM
GSMD Registrar's Suite, DHMC
All investigators and research personnel must complete training in human subjects protection prior to initiating research activities. To fulfill this requirement, you can attend an in-person training session, or complete an online tutorial.
|Jan 27||3 - 4 PM||DHMC, Aud A|
|Feb 24||3 - 4 PM||DHMC, Aud C|
|Mar 24||3 - 4 PM||DHMC, Aud C|
|Apr 28||3 - 4 PM||DHMC, Aud C|
|May 26||3 - 4 PM||DHMC, Aud A|
*Dates/times are subject to change. Please note that each session must have three participants registered or it will be cancelled. Please register for a training session by sending an email message to CPHS.Tasks@Dartmouth.edu
To complete the CITI (Collaborative IRB Training Initiative) online option, register at the following URL: http://www.citiprogram.org/ and complete either the Group 1 Biomedical or Group 2 Social/Behavioral Basic Course. CPHS also accepts the Group 3 Biomedical Data or Specimens Only Research course for researchers only working with biomedical data or specimens. Please contact our office for further guidance, 603-646-6482.
Note: CPHS training is required for all individuals responsible for the design, conduct, or reporting of human subject research.
If you are also involved in clinical research please complete The Good Clinical Practice module as required by the Clinical Trials Office.
If you are receiving funds from the National Science Foundation you are required to complete a Responsible Conduct of Research (RCR) module
Last Updated: 1/13/15