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 Quintiles and Sponsor for Sponsor’s use. Site shall afford Sponsor and Quintiles and their representatives and designees reasonable access to Site’s facilities and to Medical Records and Study Data so as to permit Sponsor and Quintiles 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 Quintiles and Sponsor for Sponsor’s use. Site shall afford Sponsor and Quintiles and their representatives and designees reasonable access to Site’s facilities and to Medical Records Records, Study Data, other source documents and Study Data all required licenses, certificates and accreditations so as to permit Sponsor and Quintiles 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 Quintiles and Sponsor for Sponsor’s use. Site shall afford Sponsor and Quintiles and their representatives and designees reasonable access to Site’s facilities and to Medical Records and Study Data so as to permit Sponsor and Quintiles and their representatives and designees to monitor the Study. Access to Medical Records will be granted in a manner consistent with the applicable provisions of Act No. 372/2011 Coll., On Healthcare Services.

Access, Use, Monitoring and Inspection. Site shall provide original or copies (as the case may be) of all Study Data to Quintiles and Sponsor for Sponsor’s use. Site shall afford Sponsor and Quintiles and their representatives and designees reasonable assistance and reasonable access to Site’s facilities and to Medical Records and Study Data so as to permit Sponsor and Quintiles and their representatives and designees to monitor the Study1.

Access, Use, Monitoring and Inspection. Site shall provide original or copies (as the case may be) of all Study Data to Quintiles and Sponsor for Sponsor’s use. In addition, and without limitation on the foregoing, Site shall afford Sponsor and Quintiles and their representatives and designees reasonable access to Site’s facilities and to Medical Records and Study Data so as to permit Sponsor and Quintiles 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 Quintiles and Sponsor for Sponsor’s use. Site shall afford Sponsor and Quintiles Xxxxxxxxx and their representatives and designees reasonable assistance and reasonable access to Site’s facilities and to Medical Records and Study Data so as to permit Sponsor and Quintiles and their representatives and designees to monitor the StudyStudy within the Institution’s working hours (7 a.m. – 3.30 p.m.).

Access, Use, Monitoring and Inspection. Site shall provide original or copies (as the case may be) of all Study Data to Quintiles and Sponsor for Sponsor’s use. Site shall afford Sponsor and Quintiles and their representatives and designees reasonable direct access to Site’s facilities and to Medical Records Records. Study Data, procedures and records related to the Study Data (clinical and financial) so as to permit Sponsor and Quintiles and their representatives and designees to audit and monitor the Study.

Access, Use, Monitoring and Inspection. Upon Quintiles’ or Sponsor’s request, Site shall provide original or copies (as the case may be) of all Study Data Documentation to Quintiles and Sponsor for Sponsor’s use. Site shall afford Sponsor and Quintiles 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 Quintiles 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 Quintiles and Sponsor for Sponsor’s use. Site shall afford Sponsor and Quintiles and their representatives and designees reasonable access to Site’s facilities and to Medical Records and Study Data so as to permit Sponsor and Quintiles and their representatives and designees to monitor the Study.záznamech před jejich vložením do CRF. Místo provádění klinického hodnocení zajistí neprodlené předkládání CRFs; a