Testing of Product Sample Clauses

Testing of Product. Prior to release of Product to finished goods inventory or release for Delivery to Prometheus, GSK shall test the Products for Nonconformities (as defined below), in accordance with the testing procedures described in the Specifications and the Quality Agreement and as otherwise required by cGMPs, Applicable Laws and Regulatory Acts. GSK shall provide Prometheus with a Certificate of Analysis for each batch of Product shipped to Prometheus.

Testing of Product. (a) Upon receival of a Consignment at the Facility, QBT will test the Product to determine: (i) its type and Grade; and (ii) its Receival Tonnage. (b) QBT may undertake any testing, including the following, to determine the type and Grade of a Consignment: (i) protein, moisture and contaminant testing; (ii) falling number testing; (iii) test weight; and (iv) Other items so specified by Client and agreement by QBT (c) QBT defines 'nil' as less than 0.01% by weight where a 'nil' tolerance is specified in the approved receivals. (d) QBT will undertake all testing in accordance with Good Operating Practice, using instruments which comply with the provisions of the National Measurement Act 1960 (Cth) and National Measurement Regulations 1999 (Cth). (e) In the absence of manifest error, QBT's testing results will (for the purposes of this Agreement) be taken to be conclusive evidence of the matters to which they relate. (f) Within 1 Business Day of receipt, QBT will deliver a statement to the Client specifying the type, grade and weight determinations made by QBT for each Consignment received at the Facility.

Testing of Product. Distributor shall conduct the testing of the Product as set forth on Exhibit B.

Testing of Product. GENETHON will perform certain in-process testing and final Product testing according to the detail of the Master Batch Record and Specifications. The full analytical testing results including in process control and final product QC results will be part of the Manufacturing Batch Record available for review on site GENSIGHT. GENSIGHT will be informed of Product which does not meet Specifications prior to edition of validated Certificate of Analysis and therefore shipment to GENSIGHT. Product not meeting requirements as defined in the Master Batch Record and Specifications will not be released to GENSIGHT except by request from and with approval by GENSIGHT.

Testing of Product. OWNER has the right to require that the LICENSED PRODUCT be submitted to testing by a testing laboratory approved by OWNER, at LICENSEE’s cost, and in accordance with generally accepted testing methods, protocols and standards. OWNER will seek to conduct any such inspection and/or testing in a manner calculated to reasonably minimize interference with normal business operations. No such inspection or testing will reduce, mitigate or eliminate any of LICENSEE’s obligations under this AGREEMENT.

Testing of Product. REVIEW AND STORAGE OF RAW DATA AND REPORTS ....................................................

Testing of Product. 2.1. Sampling, Inspection, and Testing of PRODUCT 2.2. Batch Release 2.3. Stability Program 2.4. Annual Quality Review

Testing of Product. 2.1. Sampling, Inspection, and Testing of PRODUCT 2.1.1 The sampling, inspection, and testing of in-process material related to the PRODUCT shall be carried out by APO according to the product specifications and shall be appropriately documented. 2.1.2 APO shall sample the PRODUCT per APO procedures. 2.1.3 APO is responsible for quality control (QC) testing of the PRODUCT. 2.1.4 APO shall perform final PRODUCT testing per the test methods and specifications agreed upon between APO and GILEAD.

Testing of Product. Tests to be carried out are specified in Annex D. On CONTRACT GIVER's demand (confirmed in writing) additional tests and deviant testing instructions may be used for individual analytical orders. The deviant testing instructions will either be provided by CONTRACT GIVER or by CONTRACT LABORATORY after mutual consent. If not otherwise agreed CONTRACT LABORATORY shall run testing to the extent specified in the analytical order and according to the test methods referenced in Annex D using the test equipment described there. The extent of method transfer and validation is in the responsibility of CONTRACT GIVER and is only performed on CONTRACT GIVER's written demand.

Testing of Product. Prior to release of API, FIS shall test the API in accordance with the testing procedures described in the Specifications, and shall provide Purchaser with a completed Batch Record, a Certificate of Analysis (“CofA”), a Certificate of Conformance (“CofC”) and any other raw data or documents requested by Purchaser as agreed upon in the Quality Agreement for each batch of API.