During and after completion of the Study, the Contracting. Partners shall submit to the Company all documents received from authorities, ethics committee/s, and/or competent regulatory authorities regarding any consent or authorization or safety- related communication with respect to the Study within 24 hours following their receipt.
Appears in 2 contracts
During and after completion of the Study, the Contracting. Partners shall submit to the Company Sponsor all documents received from authorities, ethics committee/s, and/or competent regulatory authorities regarding any consent or authorization or safety- related communication with respect to the Study within 24 hours following their receipt.
Appears in 1 contract
Samples: Clinical Trial Agreement
During and after completion of the Study, the Contracting. Partners shall submit to the Company Sponsor all documents received from authorities, ethics committee/s, and/or competent regulatory authorities regarding any consent or authorization or safety- without undue delay and safety related communication with respect to the Study within 24 hours following their receipt.
Appears in 1 contract
Samples: Clinical Trial Agreement
During and after completion of the Study, the Contracting. Partners shall submit to the Company Sponsor all documents received from authorities, ethics committee/s, and/or competent regulatory authorities regarding any consent or authorization or safety- related communication with respect to the Study within 24 hours following their receipt.,
Appears in 1 contract
Samples: Clinical Trial Agreement