Common use of Records Maintenance and Retention Clause in Contracts

Records Maintenance and Retention. Institution will maintain adequate and accurate records relating to the disposition of the Trial Drug and the performance of all required Protocol procedures on Trial subjects, including but not limited to, written source documents, medical records, charts pertaining to individual Trial subjects, “Case Report Forms” (“CRFs”), accounting records, notes, reports, and data. Institution will retain these documents for the longer of: (i) at least 5 years after completion or

Appears in 1 contract

Samples: Trial Agreement

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Records Maintenance and Retention. Institution will maintain adequate and accurate records relating to the disposition of the Trial Drug and the performance of all required Protocol procedures on Trial subjects, including but not limited to, written source documents, medical records, charts pertaining to individual Trial subjects, “Case Report Forms” (“CRFs”), accounting records, notes, reports, and data. Institution will retain these documents for the longer of: (i) at least 5 years after completion or,

Appears in 1 contract

Samples: Trial Agreement

Records Maintenance and Retention. Investigator and Institution will maintain adequate and accurate records relating to the disposition of the Trial Drug and the performance of all required Protocol procedures on Trial subjects, including but not limited to, written source documents, medical records, charts pertaining to individual Trial subjects, “Case Report Forms” (“CRFs”), accounting records, notes, reports, and data. Institution and Investigator will retain these documents for the longer of: (i) at least 5 years after completion oror earlier termination of the Trial at all participating institutions; (ii) 2 years

Appears in 1 contract

Samples: www.hlidacstatu.cz

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Records Maintenance and Retention. Institution will maintain adequate and accurate records relating to the disposition of the Trial Drug and the performance of all required Protocol procedures on Trial subjects, including but not limited to, written source documents, medical records, charts pertaining to individual Trial subjects, “Case Report Forms” (“CRFs”), accounting records, notes, reports, and data. Institution will retain these documents for the longer of: (i) at least 5 years after completion oror earlier termination of the Trial at all participating

Appears in 1 contract

Samples: Trial Agreement

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