Access, Use, Monitoring and Inspection. Institution shall provide original or copies (as the case may be) of all Study Data to Quintiles and Sponsor for Sponsor’s use. Institution shall afford Sponsor and Quintiles and their representatives and designees reasonable access to Institution ’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. Institution shall afford regulatory authorities reasonable access to Institution ’s facilities and to Medical Records and Study Data, and the right to copy Medical Records and Study Data. The Institution agrees to cooperate with the representatives of Quintiles and Sponsor who visit the Institution, and the Institution agrees to ensure that the employees, agents and representatives of the Institution do not harass, or otherwise create a hostile working environment for such representatives. The Institution shall immediately notify Quintiles of, and provide Quintiles copies of, any inquiries, correspondence or communications to or from any governmental or regulatory authority relating to the Study, including, but not limited to, requests for inspection of the Institution’s facilities, and the Institution shall permit Quintiles and Sponsor to attend any such inspections. The Institution will make reasonable efforts to separate, and not disclose, all Confidential Information that is not required to be disclosed during such inspections.
Appears in 3 contracts
Samples: Clinical Trial Agreement, Clinical Trial Agreement, Clinical Trial Agreement
Access, Use, Monitoring and Inspection. Institution shall provide original or copies (as the case may be) of all Study Data to Quintiles and Sponsor for Sponsor’s use. Institution shall afford Sponsor and Quintiles and their representatives and designees reasonable access to Institution ’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. Institution shall afford regulatory authorities reasonable access to Institution ’s facilities and to Medical Records and Study Data, and the right to copy Medical Records and Study Data. The Institution agrees to cooperate with the representatives of Quintiles and Sponsor who visit the Institution, and the Institution agrees to ensure that the employees, agents and representatives of the Institution do not harass, or otherwise create a hostile working environment for such representatives. The Institution shall immediately notify Quintiles of, and provide Quintiles copies of, any inquiries, correspondence or communications to or from any governmental or regulatory authority relating to the Study, including, but not limited to, requests for inspection of the Institution’s facilities, and the Institution shall permit Quintiles and Sponsor to attend any such inspections, to the extent not prohibited by such governmental or regulatory authority. The Institution will make reasonable efforts to separate, and not disclose, all Confidential Information that is not required to be disclosed during such inspections. nařízení.
Appears in 1 contract
Samples: Clinical Trial Agreement
Access, Use, Monitoring and Inspection. Institution shall provide original or copies (as the case may be) of all Study Data to Quintiles and Sponsor for Sponsor’s use. Institution shall afford Sponsor and Quintiles and their representatives and designees reasonable access to Institution ’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. Institution shall afford regulatory authorities reasonable access to Institution ’s facilities and to Medical Records and Study Data, and the right to copy Medical Records and Study Data. The Institution agrees to cooperate with the representatives of Quintiles and Sponsor Xxxxxxx who visit the Institution, and the Institution agrees to ensure that the employees, agents and representatives of the Institution do not harass, or otherwise create a hostile working environment for such representatives. The Institution shall immediately notify Quintiles of, and provide Quintiles copies of, any inquiries, correspondence or communications to or from any governmental or regulatory authority relating to the Study, including, but not limited to, requests for inspection of the Institution’s facilities, and the Institution shall permit Quintiles and Sponsor to attend any such inspections. The Institution will make reasonable efforts to separate, and not disclose, all Confidential Information that is not required to be disclosed during such inspections.
Appears in 1 contract
Samples: Clinical Trial Agreement
Access, Use, Monitoring and Inspection. Institution Site shall provide original or copies (as the case may be) of all Study Data to Quintiles and Sponsor for Sponsor’s use. Institution Site shall afford Sponsor and Quintiles and their representatives and designees reasonable access to Institution 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. Institution To the extent required by applicable legal regulations, Site shall afford regulatory authorities reasonable access to Institution Site’s facilities and to Medical Records and Study Data, and the right to copy Medical Records and Study Data. The Institution Site agrees to cooperate with the representatives of Quintiles and Sponsor who visit the InstitutionSite, and the Institution Site agrees to ensure that the employees, agents and representatives of the Institution Site do not harass, or otherwise create a hostile working environment for such representatives. The Institution Site shall immediately notify Quintiles of, and provide Quintiles copies of, any inquiries, correspondence or communications to or from any governmental or regulatory authority relating to the Study, including, but not limited to, requests for inspection of the InstitutionSite’s facilities, and the Institution Site shall permit Quintiles and Sponsor to attend any such inspections. The Institution Site will make reasonable efforts to separate, and not disclose, all Confidential Information that is not required to be disclosed during such inspections.
Appears in 1 contract
Samples: Clinical Trial Agreement
Access, Use, Monitoring and Inspection. Institution shall provide original or copies (as the case may be) of all Study Data to Quintiles and Sponsor for Sponsor’s use. Institution shall afford Sponsor and Quintiles and their representatives and designees reasonable access to Institution ’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. Institution shall afford regulatory authorities reasonable access to Institution Institution’s facilities and to Medical Records and Study Data, and the right to copy Medical Records and Study Data. The Institution agrees to cooperate with the representatives of Quintiles and Sponsor who visit the Institution, and the Institution agrees to ensure that the employees, agents and representatives of the Institution do not harass, or otherwise create a hostile working environment for such representatives. The Institution shall immediately notify Quintiles of, and provide Quintiles copies of, any inquiries, correspondence or communications to or from any governmental or regulatory authority relating to the Study, including, but not limited to, requests for inspection of the Institution’s facilities, and the Institution shall permit Quintiles and Sponsor to attend any such inspections. The Institution will make reasonable efforts to separate, and not disclose, all Confidential Information that is not required to be disclosed during such inspections.
Appears in 1 contract
Samples: Clinical Trial Agreement
Access, Use, Monitoring and Inspection. Institution shall provide original or copies (as the case may be) of all Study Data to Quintiles and Sponsor for Sponsor’s use. Institution shall afford Sponsor and Quintiles and their representatives and designees reasonable access to Institution Institution’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. Institution shall afford regulatory authorities reasonable access to Institution Institution’s facilities and to Medical Records and Study Data, and the right to copy Medical Records and Study Data. The Institution agrees to cooperate with the representatives of Quintiles and Sponsor who visit the Institution, and the Institution agrees to ensure that the employees, agents and representatives of the Institution do not harass, or otherwise create a hostile working environment for such representatives. The Institution shall immediately notify Quintiles of, and provide Quintiles copies of, any inquiries, correspondence or communications to or from any governmental or regulatory authority relating to the Study, including, but not limited to, requests for inspection of the Institution’s facilities, and the Institution shall permit Quintiles and Sponsor to attend any such inspections. The Institution will make reasonable efforts to separate, and not disclose, all Confidential Information that is not required to be disclosed during such inspections.
Appears in 1 contract
Samples: Clinical Trial Agreement