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. 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
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