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. 1.3.3

Appears in 4 contracts

Samples: Trial Agreement, Clinical Trial Agreement, Clinical Trial Agreement

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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

Samples: Clinical Trial Agreement Zmluva O Klinickom

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

Samples: Trial Agreement Smlouva O Klinickém Hodnocení

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

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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

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