Study Data. Institution and Investigator shall record and maintain complete medical records (including, without limitation, case report forms, laboratory work sheets and reports, and all relevant source documents) generated as a result of conducting the Study (collectively, the “Study Data”) in a timely, accurate, complete and legible manner in the form described in the Protocol.
Appears in 3 contracts
Sources: Clinical Trial Agreement, Clinical Trial Agreement, Clinical Trial Agreement
Study Data. (a) Study Data. Institution shall ensure that the Investigator keeps and Investigator shall record and maintain maintains complete medical records (including, without limitation, case report forms, laboratory work sheets and reports, and all relevant source documents) generated as a result of conducting the Study (collectively, the “Study Data”) in a timely, accurate, complete and legible manner in the form described in the Protocol.
Appears in 2 contracts
Study Data. Institution and Investigator shall record and maintain complete medical records (including, without limitation, case report forms, laboratory work sheets and reports, and all relevant source documents) generated as a result of conducting the Study (collectively, the “Study Data”) in a timely, accurate, complete and legible manner in the form described in the Protocol.with (a)
Appears in 1 contract
Sources: Clinical Trial Agreement