Common use of During and after completion of the Study, the Contracting Clause in Contracts

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

Samples: Clinical Trial Agreement, 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

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