Quality Assurance and Control. To the extent applicable, the Site Parties shall permit the Study Monitor, Auditor, IRB and any official with a legal right to inspect and access all relevant documentation and source data for monitoring of the progress of the Clinical Study, the proper collection and recording of Clinical Study data, and altogether the good quality of the Clinical Study and compliance with applicable Law. Parties will make in good faith arrangements concerning the planning and follow-up of such audits or inspections.
Appears in 2 contracts
Sources: Clinical Study Site Agreement, Clinical Study Site Agreement
Quality Assurance and Control. To the extent applicable, the Site Parties shall permit the Study Monitor, Auditor, IRB the Ethics Committee and any official with a legal right to inspect and access all relevant documentation and source data for monitoring of the progress of the Clinical Study, the proper collection and recording of Clinical Study data, and altogether the good quality of the Clinical Study and compliance with applicable Law. Parties will make in good faith arrangements concerning the planning and follow-up of such audits or inspections.
Appears in 1 contract
Sources: Clinical Study Site Agreement