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