Case Report Forms. [***] is responsible for the development and subsequent revisions of case report forms for Clinical Studies (“CRF”) subject to review and approval of the CSOG. Sponsor will be responsible for distributing the CRFs and any amendments to the CRFs to all Participating Sites in a timely manner. For each Clinical Study conducted at MSKCC, MSKCC shall prepare and maintain CRFs and other patient records and case histories with all pertinent data documented as required by the applicable Study Protocol. Sponsor shall not disclose patient names, except to the extent that the patient consent form permits or as required by applicable law or regulation. All CRFs shall be owned by Sponsor.
Appears in 3 contracts
Sources: Master Clinical Study Agreement, Master Clinical Study Agreement (Juno Therapeutics, Inc.), Master Clinical Study Agreement (Juno Therapeutics, Inc.)