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Dear SOM Clinical Research Community,


The SOM CRSO is in the process of developing a portfolio of Standard Operating Procedures (SOPs) widely applicable to clinical research conducted across the SOM to achieve efficient and consistent workflows, ensure regulatory compliance, and realize best operational practices in clinical research.  As an individual who may be responsible for conducting processes covered by the SOPs, we are inviting you to be a reviewer of these SOPs. Your feedback is very important in ensuring that that the SOPs are appropriate and simple to follow.


The first SOP we would like your feedback on is the SOM SOP 501.1: Obtaining and Documenting Informed Consent. This SOP provides step-by-step procedures for obtaining and documenting written informed consent from adult research participants or participants’ legally authorized representatives.


  • To review the SOP and submit feedback, please view the online survey. The survey will be available until August 20, 2021, at 5pm.
  • You may click here to view the draft SOP directly without accessing the feedback survey. 


If you have general questions about the SOM SOP development process, please review the SOP page of the CRSO website.


Thank you in advance for your time and for providing this important feedback!