NIH CRM Template Consent Form — Reference the NIH CRM template consent when collecting tissue for use in iPSC research to ensure that iPSC lines can be freely transferred among collaborators, used in future research, banked in a repository, etc. All materials need to be approved by your Institutional Review Board (IRB).
Limited Use Label License (LULL) — Review all restrictions placed on cells derived using each reagent and ensure they do not overly restrict the future use of your work.
Material Transfer Agreement (MTA) — Carefully review all MTAs to ensure you relevant issues are considered when obtaining iPSC lines and/or reagents used to generate/manipulate iPSCs.
iPSC Checklist — Required registration document for IRP investigators that generate or obtain iPSC lines.
Obtain Office of Human Subjects Research (OHSR) — OHSR review request form, If OHSR exemption is not an option, you will need to get IRB approval.