Access, Use, Monitoring and Inspection. Site shall provide (through the CRF) original or copies (as the case may be) of all Study Data to IQVIA and Sponsor for Sponsor’s use. Site shall afford Sponsor and IQVIA and affiliates, their representatives and designees reasonable access to Site’s facilities and to Medical Records and Study Data so as to permit Sponsor and IQVIA and affiliate, their representatives and designees to monitor the Study and audit Site’s and Study Staff’s conduct of the Study. Institution and Investigator shall cooperate with and facilitate such visit. 1.3.3
Appears in 3 contracts
Samples: Clinical Trial Agreement, Trial Agreement, Trial Agreement
