Common use of Access, Use, Monitoring and Inspection Clause in Contracts

Access, Use, Monitoring and Inspection. Site shall provide 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 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 their representatives and designees to monitor the Study.

Access, Use, Monitoring and Inspection. Site shall provide 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 their representatives and designees reasonable access to Site’s facilities and to Medical Records and Study Data as well as to any other documents and documentation so as to permit Sponsor and IQVIA and their representatives and designees to monitor the StudyStudy and compliance with this Agreement.

Access, Use, Monitoring and Inspection. Site shall provide original originals 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 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 their representatives and designees to monitor the Study. At the request of Sponsor or IQVIA, Site shall promptly correct any errors or omissions in the Study Data.

Access, Use, Monitoring and Inspection. Upon IQVIA’ or Sponsor’s request, Site shall provide original or copies (as the case may be) of all Study Data Documentation to IQVIA and Sponsor for Sponsor’s use. Site shall afford Sponsor and IQVIA and their representatives and designees reasonable access to Site’s facilities and to Medical Records and Study Data Documentation so as to permit Sponsor and IQVIA and their representatives and designees to monitor the Study.

Access, Use, Monitoring and Inspection. Site shall provide 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 their representatives and designees with an in advanced agreed date reasonable access to Site’s facilities and to Medical Records and Study Data so as to permit Sponsor and IQVIA and their representatives and designees to monitor the Study.

Access, Use, Monitoring and Inspection. Upon reasonable request, Site shall provide 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 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 their representatives and designees to monitor and observe the conduct of the Study.

Access, Use, Monitoring and Inspection. Site shall provide 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 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 their representatives and designees to monitor the Study.and

Access, Use, Monitoring and Inspection. Site shall provide original or copies (as the case may be) of all Study Data to IQVIA and Sponsor for Sponsor’s use. Site shall shall, subject to prior agreement, afford Sponsor and IQVIA and 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 their representatives and designees to monitor the Study.monitor

Access, Use, Monitoring and Inspection. Site shall provide 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 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 their representatives and designees to monitor the Study. The Parties agree that the Sponsor shall have the right to audit the Study records during and subsequent to the Study.

Access, Use, Monitoring and Inspection. Site shall provide 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 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 their representatives and designees to monitor the Study1.