Quality Assurance and Control. 6.1. The Site Parties shall ensure that all procedures defined in the Protocol are complied with, so that all data generated at the Trial Site are reliable and have been processed correctly (especially the randomization lists, and the blind character of the Clinical Trial as the case may be) and will ensure that the content of the CRFs or e-CRFs will accurately reflect source documents.
Appears in 4 contracts
Samples: Trial Agreement (Lixte Biotechnology Holdings, Inc.), Trial Agreement, Trial Agreement
