Record Management. 1.4.1 Institution/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 the period as required by law or any regulatory requirements.
Appears in 3 contracts
Samples: Clinical Trial Agreement, Clinical Trial Agreement, Clinical Trial Agreement
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 af period of time according to applicable law. Sponsor will provide instructions for the period as required by law retention or any regulatory requirementsdestruction of documentation.
Appears in 1 contract
Samples: Clinical Trial Agreement
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 the a period as required by law or any regulatory requirementsof time according to applicable law.
Appears in 1 contract
Samples: Standard Clinical Trial Agreement