Records and Samples. To the extent not otherwise transferred to the County's possession, Xxxx agrees to retain and provide the County with reasonable access to all work product, records, papers and other documents involving transactions and work related to or performed under this agreement for a period of three (3) years after this agreement expires. When services involve testing or sampling, Xxxx agrees to either retain all test products or samples collected by or submitted to Firm, or return same to the County as mutually agreed upon. In absence of agreement, Firm shall not dispose of test samples or products without notice to or consent by the County or the County's representative.
Records and Samples. To the extent not otherwise transferred to the City's possession, Consultant agrees to retain and provide the City with reasonable access to all work product, records, papers and other documents involving transactions and work related to or performed under this agreement for a period of three (3) years after this agreement expires. When services involve testing or sampling, Consultant agrees to either retain all test products or samples collected by or submitted to Consultant, or return same to the City as mutually agreed upon. In absence of agreement, Consultant shall not dispose of test samples or products without notice to or consent by the City or the City's representative.
Records and Samples. Supplier shall maintain all records relating to its obligations hereunder as required by current Good Manufacturing Practices (“cGMPs”) and current Good Laboratory Practices (“cGLPs”), as applicable, and Applicable Law for such time periods referenced thereby. Supplier shall make such records available to Purchaser for Purchaser’s inspection and copying promptly following a written request by Purchaser. In addition, Supplier shall retain a file sample properly stored from each lot or batch of Licensed Adjuvants supplied to Purchaser hereunder in accordance with cGMPs.
Records and Samples. (a) Unless otherwise required by law or by the terms of this Agreement or the relevant IPA, all such Sponsor property, including but not limited to written records pertaining to a Study, which CRU shall have in its possessions shall be maintained by CRU for a period of not less than five (5) years from commencement of archiving and shall be organized in such manner that it will be ready for prompt reference. After five (5) years or such longer period as may be required by applicable laws or regulations, CRU may dispose of such property in accordance with Sponsor’s instructions and at Sponsor’s expense, and in any event, additional storage of Sponsor property after five (5) years shall be at Sponsor’s expense. If Sponsor fails to give said instructions, CRU shall so notify Sponsor; and if said instructions are still not forthcoming within thirty (30) days of said notification, then CRU may destroy such property as it determines.
(b) Primary pharmacokinetic samples will be shipped to the appropriate analytical laboratory according to Sponsor/protocol requirements. Secondary samples will be stored with CRU according to the Sponsor/protocol requirements for six (6) months following last subject clinical visit at which time the samples will be shipped to the archive facility of the Sponsor’s choice at Sponsor’s expense. The Sponsor shall maintain written records of any disposition of the samples in accordance with applicable laws and regulations. In the event the Sponsor fails to indicate archive facility, secondary pharmacokinetic samples will be disposed of by CRU. The return or destruction of Active Pharmaceutical Ingredient (API) will be specified within the Study Protocol.
Records and Samples. PowderJect shall ensure that complete, accurate, and authentic accounts, notes, product stability records, quality control records, batch release records, deviation reports, batch records, data, and all other records pertaining to the Manufacture, processing, labeling, storage, testing, and distribution of the Gas Cylinders supplied hereunder are kept in accordance with applicable laws and regulations, including, without limitation, master production and control records. In addition, PowderJect shall ensure that samples of Gas Cylinders from each batch manufactured pursuant to this Agreement are retained after AlgoRx's acceptance of each such batch. PowderJect shall ensure that such records and samples are retained for a period of six (6) years following the date of Manufacture, or longer if required by law, and, upon request, shall make available to AlgoRx copies of such records and portions of the samples at AlgoRx's expense. After such time period, PowderJect shall deliver such records and samples to AlgoRx.
Records and Samples. Shionogi shall maintain (or cause to be maintained) complete, accurate, and authentic accounts, notes, data, and records pertaining to its manufacture, processing, Quality Control Procedure test results, and packaging of the Clinical Samples in accordance with [*].
Records and Samples. (a) The Supplier must keep in writing true and accurate records of such information as Xxxxxxx or a2MCA may reasonably request from time to time be retained including records relating to the raw A2 Beta Casein Protein Milk and that the Supplier supply to Brownes and make all such records available to Xxxxxxx, a2MCA (or any authorised representative of a2MCA) when requested to do so.
Records and Samples. IsoRay shall keep, or cause to be kept, complete, accurate and authentic accounts, notes, data and records pertaining to the manufacture, processing, testing, labeling, storage, and distribution of the Products, including without limitation master production and control records, in accordance with applicable laws and regulations. IsoRay shall retain, or cause to be retained, such records for a period of five (5) years following the date of manufacture, or longer if required by law, and upon request, shall make available to GT MED TECH copies of such records. After such time period, IsoRay shall notify GT MED TECH prior to the destruction of any records retained under this Section 8.5 and, at GT MED TECH’s request, shall transfer such records to GT MED TECH.
Records and Samples. Written records shall be kept by the producing laboratory of all steps in the production and control of blood-grouping reagents. Adequate samples of all reagents issued shall be retained by the laboratory until it can be reasonably assumed that the batch is no longer in use.
Records and Samples. Halo shall maintain reserve samples and batch production records in accordance with Applicable Law;
