Stability test Clause Samples

A stability test clause defines the requirements and procedures for assessing whether a product, material, or system maintains its intended performance and characteristics over a specified period or under certain conditions. Typically, this clause outlines the testing methods, duration, and acceptance criteria that must be met to demonstrate stability, such as storing a pharmaceutical product at various temperatures and checking for changes in efficacy or safety. Its core practical function is to ensure that the subject of the contract remains reliable and safe throughout its expected lifecycle, thereby minimizing risks associated with degradation or failure.
Stability test. The stability of a vehicle shall be such that the point at which overturning occurs would not be passed if the surface on which the vehicle stands were tilted to both sides in turn to an angle of 28 degrees from the horizontal.
Stability test. Both before and after heating the final liquid product or reconstituted dried product at 37° C. for 7 days there should be no visible evidence of precipitation or turbidity. Moreover, after heating at 57° C. for 4 hours there should be no visible evidence of gelation. Loss of weight on drying – When dried over phosphorus pentoxide at a pressure not exceeding 0.02 mm. of mercury for 24 hours it must not lose more than 0.5 per cent of its weight. Storage – The dried human gamma globulin must be kept in an atmosphere of nitrogen or in a vacuum in a sterile container sealed so as to exclude micro-organisms and, as far as possible, moisture, protected from light and stored at a temperature below 20° C. Labelling – The label on the container shall state
Stability test. Following the completion of the A▇▇▇▇tance Test, PARTNER shall perform a stability test for 14 (fourteen) days for the purposes of examining the performance of the Sub-Ring System or Sub Sub-Ring System in whole and of ensuring that the Work relating to such Sub-Ring System or Sub Sub-Ring System has been technically performed in accordance with the Technical Specification under this Agreement. During such examination, the Parties are not allowed to make any adjustment in case of any irregularity arising in certain part of the Sub-Ring System or Sub Sub-Ring System.
Stability test. In order to determine the stability of the nanoparticles made by the PEC and ionotropic gelation methods, the freeze-dried samples, kept at −4.0 ◦C, were analyzed monthly for 6 months and the amount of insulin was measured using HPLC. Briefly, 1.0 mg of freeze-dried samples was analyzed for the insulin content and the results were compared with the initial loading obtained on the first day of the experiment.
Stability test. In accordance with the provisions set forth in Development Supply Agreement or the Commercial Supply Agreement, as the case may be, and unless otherwise agreed between the Parties, VectivBio shall conduct the stability test (including stress testing drug product (e.g., Freeze and Thaw cycle Test, Accelerated Test)) of the Compound and the Product (in what form to be defined in the Commercial Supply Agreement or the Commercial Quality Agreement) during the whole period of clinical trials and commercial sale in the Territory. VectivBio shall provide AKP with the results of such tests in a timely manner as a part of providing VectivBio Know-How and Materials.
Stability test. Upon the completion of ACCEPTANCE T▇▇▇, PARTNER shall conduct a stability test for the period of ten

Related to Stability test

  • Stability Testing Patheon will conduct stability testing on the Products in accordance with the protocols set out in the Specifications for the separate fees and during the time periods set out in Schedule C. Patheon will not make any changes to these testing protocols without prior written approval from Client. If a confirmed stability test failure occurs, Patheon will notify Client within [***], after which Patheon and Client will jointly determine the proceedings and methods to be undertaken to investigate the cause of the failure, including which party will bear the cost of the investigation. Patheon will not be liable for these costs unless it has failed to perform the Manufacturing Services in accordance with the Specifications and cGMPs. Patheon will give Client all stability test data and results at Client’s request.

  • Test The outer surface of the lamp lenses shall be subjected once or more than once to the action of the sand jet produced as described above. The jet shall be sprayed almost perpendicular to the surface to be tested. The deterioration shall be checked by means of one or more samples of glass placed as a reference near the lenses to be tested. The mixture shall be sprayed until the variation in the diffusion of light on the sample or samples measured by the method described in Appendix 2, is such that: Δ d = (T5 - T4) / T2 ≤ 0.0250 ± 0.0025 Several reference samples may be used to check that the whole surface to be tested has deteriorated homogeneously.

  • Laboratory Testing All laboratories selected by UPS Freight for analyzing Controlled Substances Testing will be HHS certified.

  • Performance Testing (a) All performance tests of the Project, including any Initial Performance Test required in Section 2 of Appendix VIII, will be performed in accordance with the test procedures set forth in Appendix VIII (“Performance Test”), including additional procedures and protocols related to Performance Testing as mutually agreed between Buyer and Seller (“Test Procedures”). Seller shall bear all costs and receive all revenues, if applicable, associated with all Performance Tests. (b) After the Initial Delivery Date and during the Delivery Term, Buyer will have the right to conduct a Performance Test (“Buyer Performance Test”) no more than once a calendar year to demonstrate whether the Project is capable of delivering the Distribution Services at the Contract Capacity. Within 30 calendar days following a Buyer Performance Test, Seller will have the right to retest the Project with a Performance Test (“Seller Retest”). For the avoidance of doubt, the results of any Seller Retest will supersede the results of the preceding Buyer Performance Test. (i) If a Buyer Performance Test or, if a corresponding Seller Retest has occurred, a Seller Retest demonstrates the Project is capable of delivering Distribution Services at or above ninety-nine percent (99%) of the Initial Contract Capacity, the Contract Capacity will remain the Initial Contract Capacity; (ii) If a Buyer Performance Test or, if a corresponding Seller Retest has occurred, a Seller Retest demonstrates the Project is capable of delivering Distribution Services at more than or equal to eighty-five (85%) of the Initial Contract Capacity, but less than ninety-nine percent (99%) of the Initial Contract Capacity (“Testing Band”), the Contract Capacity will be automatically adjusted (upwards or downwards) to the capacity commensurate with the amount of Distribution Services the Project delivered during the Performance Test within the Testing Band. (iii) If a Buyer Performance Test or, if a corresponding Seller Retest has occurred, a Seller Retest demonstrates the Project is not capable of delivering Distribution Services of at least eighty-five percent (85%) of the Initial Contract Capacity, an Event of Default shall occur in accordance with Section 7.1(a)(viii).

  • Random Testing Notwithstanding any provisions of the Collective Agreement or any special agreements appended thereto, section 4.6 of the Canadian Model will not be applied by agreement. If applied to a worker dispatched by the Union, it will be applied or deemed to be applied unilaterally by the Employer. The Union retains the right to grieve the legality of any imposition of random testing in accordance with the Grievance Procedure set out in this Collective Agreement.