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Common use of DATA ARCHIVAL Clause in Contracts

DATA ARCHIVAL. 7.1. After completion of the Trial, Sponsor will provide the Investigator with a CD-ROM containing the entered and signed data for all Trial Participants of his/her site, including the audit trail / discrepancy details. Investigator will confirm the receipt, as well as the verification of completeness and correctness of the data contained on the CD-ROM to Sponsor. Investigator will archive the CD-ROM as part of the ISF file, to be readily available for audit and inspection purposes.

Appears in 5 contracts

Samples: Individual Clinical Trial Agreement, Clinical Trial Agreement, Clinical Trial Agreement

DATA ARCHIVAL. 7.1. After completion of the Trial, Sponsor will provide the Investigator with a CD-CD- ROM containing the entered and signed data for all Trial Participants of his/her site, including the audit trail / discrepancy details. Investigator will confirm the receipt, as well as the verification of completeness and correctness of the data contained on the CD-ROM to Sponsor. Investigator will archive the CD-ROM as part of the ISF file, to be readily available for audit and inspection purposes.

Appears in 2 contracts

Samples: Clinical Trial Agreement, Clinical Trial Agreement

DATA ARCHIVAL. 7.1. After completion of the Trial, Sponsor will provide the Investigator with a CD-ROM containing the entered and signed data for all Trial Participants of his/her site, including the audit trail / discrepancy details. Investigator will confirm the receipt, as well as the verification of completeness and correctness of the data contained on the CD-ROM to Sponsor. Investigator will archive the CD-CD- ROM as part of the ISF file, to be readily available for audit and inspection purposes.

Appears in 1 contract

Samples: Clinical Trial Agreement

DATA ARCHIVAL. 7.1. After completion of the Trial, Sponsor will provide the Investigator with a CD-ROM containing the entered and signed data for all Trial Participants of his/her site, including the audit trail / discrepancy details. Investigator will confirm the receipt, as well as the verification of completeness and correctness of the data contained on the CD-ROM to Sponsor. Investigator will archive the CD-ROM as part of the ISF file, to be readily available for audit and inspection purposes.correctness

Appears in 1 contract

Samples: Clinical Trial Agreement