Case Report Forms. For all subjects enrolled in the Study, Institution or Investigator will complete all case report forms required for the Study in the form and/or electronic medium supplied or specified by Sponsor and/or CRO (the “CRFs”) within twenty-four (24) hours of the subject visit during the dose escalation phase and within three (3) days of the subject visit for the remainder of the Study. Institution and Investigator will not be required to disclose information in CRFs which would permit personal identification of a subject enrolled in, or a candidate for, the Study. CRFs will be provided to CRO in a timely manner as they are completed. At the request of Sponsor and/or CRO, Institution or Investigator will promptly correct any errors and/or omissions to the CRFs for the Study and will make available to Sponsor and/or CRO the corrected CRFs and supporting records for further verification.
Appears in 2 contracts
Case Report Forms. For all subjects enrolled in the Study, Institution or Investigator will complete all case report forms required for the Study in the form and/or electronic medium supplied or specified by Sponsor and/or CRO (the “CRFs”) and within twenty-four (24) hours of the subject visit during the dose escalation phase and within three (3) days of the subject visit for the remainder of the StudyStudy specified by Sponsor and/or CRO. Institution and Investigator will not be required to disclose information in CRFs which would permit personal identification of a subject enrolled in, or a candidate for, the Study. CRFs will be provided to CRO in a timely manner as they are completed. At the request of Sponsor and/or CRO, Institution or Investigator will promptly correct any errors and/or omissions to the CRFs for the Study and will make available to Sponsor and/or CRO the corrected CRFs and supporting records for further verification.
Appears in 1 contract
Sources: Clinical Trial Agreement