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. 1.3.3
Appears in 4 contracts
Samples: Trial Agreement, Clinical Trial Agreement, Clinical Trial Agreement
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. 1.3.3.
Appears in 1 contract
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. 1.3.3and
Appears in 1 contract
Samples: Clinical Trial Agreement
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. 1.3.3.
Appears in 1 contract
Samples: Clinical Trial Agreement Zmluva O Klinickom Skúšaní
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. 1.3.3
Appears in 1 contract
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. 1.3.3monitor
Appears in 1 contract
Samples: Clinical Trial Agreement
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. 1.3.3.
Appears in 1 contract
Samples: Trial Agreement
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. 1.3.3
Appears in 1 contract
Samples: Trial Agreement
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. 1.3.3.
Appears in 1 contract
Samples: Clinical Trial Agreement