Record Management. 1.4.1 Investigator will retain in a safe and secure location, one (1) copy of all printed and electronic data and reports resulting from the Study for such longer period as required by regulatory requirements. Sponsor will provide instructions for the retention or destruction of documentation. 1.4.2 If Sponsor agree, National Coordinator and Institution may store Study documents at a mutually agreed third party site at their own expense. If they want to move the Study documents to another location, the Sponsor must be notified in writing. 1.4.3 National Coordinator shall ensure that the Investigatores maintain accurate data collection and up-to-date records of all Study subjects.
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Record Management. 1.4.1 Institution/Principal Investigator will retain in a safe and secure location, one (1) copy of all printed and electronic data and reports resulting from the Study for such longer af period as required by regulatory requirementsof time according to applicable law. Sponsor will provide instructions for the retention or destruction of documentation.
1.4.2 If Sponsor agree, National Coordinator and Institution may store Study documents at a mutually agreed third party site at their own expensesite. If they want the Institution/Principal Investigator wants to move the Study documents to another location, the Sponsor must be notified in writing.
1.4.3 National Coordinator Institution/Principal Investigator shall ensure that the Investigatores maintain accurate data collection and up-to-date records of all Study subjects.
Appears in 1 contract
Sources: Clinical Trial Agreement
Record Management. 1.4.1 Institution/Site Investigator will retain in a safe and secure location, one (1) copy of all printed and electronic data and reports resulting from the Study for such longer a period as required by regulatory requirementsaccording to applicable law. Sponsor will provide instructions for the retention or destruction of documentation.
1.4.2 If Sponsor agree, National Coordinator and Institution may store Study documents at a mutually agreed third party site at their own expensesite. If they want the Institution/Site Investigator wants to move the Study documents to another location, the Sponsor must be notified in writing.
1.4.3 National Coordinator Institution/Site Investigator shall ensure that the Investigatores maintain accurate data collection and up-to-date records of all Study subjects.
Appears in 1 contract
Sources: Clinical Trial Agreement