Common use of Packaging Instructions Deviations Clause in Contracts

Packaging Instructions Deviations. Patheon will document, investigate, and resolve any deviation from approved packaging instructions or Specifications according to Patheon SOP’s. Patheon will report and obtain approval from the Client’s responsible person for DR type deviations where there is a potential to affect Product quality. Such Client approval will not be unreasonably withheld. Patheon will provide copies of all DR’s to the Client as part of the executed batch packaging record.

Appears in 3 contracts

Samples: Supply Agreement (Relypsa Inc), Supply Agreement (Relypsa Inc), Avanir Pharmaceuticals, Inc.

AutoNDA by SimpleDocs

Packaging Instructions Deviations. Patheon will document, investigate, and resolve any deviation from approved packaging instructions or Specifications according to Patheon SOP’sSOPs. Patheon will report and obtain approval from the Client’s responsible person for DR type deviations where there is a potential to affect Product quality. Such This Client approval will not be unreasonably withheld. Patheon will provide give the Client copies of all DR’s to the Client DRs as part of the executed batch packaging record.

Appears in 2 contracts

Samples: Manufacturing Services Agreement (Horizon Therapeutics Public LTD Co), Manufacturing Services Agreement (Horizon Pharma PLC)

Packaging Instructions Deviations. Patheon will document, investigate, and resolve any deviation from approved packaging instructions or Specifications according to Patheon SOP’sSOPs. Patheon will report and obtain approval from the Client’s responsible person for DR type deviations where there is a potential to affect Product quality. Such Client approval will not be unreasonably withheld. Patheon will provide give the Client copies of all DR’s to the Client as part of the executed batch packaging record.

Appears in 1 contract

Samples: Quality Agreement (Jaguar Animal Health, Inc.)

AutoNDA by SimpleDocs

Packaging Instructions Deviations. Patheon will document, investigate, and resolve any deviation from approved packaging instructions or Specifications according to Patheon SOP’sSOPs. Patheon will report and obtain approval from the Client’s responsible person for DR type deviations where there is a potential to affect Product quality. Such This Client approval will not be unreasonably withheld. Patheon will provide give the Client copies of all DR’s to the Client as part of the executed batch packaging record.

Appears in 1 contract

Samples: Product Agreement (Horizon Pharma, Inc.)

Time is Money Join Law Insider Premium to draft better contracts faster.