Test Methodology Sample Clauses
The Test Methodology clause defines the procedures and standards by which products or services will be tested to ensure they meet specified requirements. It typically outlines the types of tests to be conducted, the criteria for passing or failing, and the responsibilities of each party in the testing process. By establishing a clear and agreed-upon approach to testing, this clause helps prevent disputes over quality and performance, ensuring that deliverables conform to contractual expectations.
Test Methodology. 5.1.1. The substitution method according to ISO 11451-1, shall be used to establish the test field conditions.
5.1.2. Calibration For TLS one field probe at the vehicle reference point shall be used. For antennas four field probes at the vehicle reference line shall be used.
Test Methodology. The testing methodology to be used for both “reasonable suspicion” and random testing shall be the same as described herein and will be based on a laboratory examination of a urine specimen. Specimen collection and laboratory examination are described in Section IV, Specimen Collection and Section V, Laboratory Analysis. Laboratory analyses of urine specimens shall be restricted to those tests authorized by this policy to detect drug abuse. They shall not be used for other purposes, such as the analyses of physiological states or diseases (e.g., pregnancy, AIDS or cancer therapy).
Test Methodology. The testing methodology will be based on a laboratory examination of a urine specimen. Specimen collection and laboratory examination are described in Section IV, Specimen Collection and Section V, Laboratory Analysis. Laboratory analysis of urine specimens shall be restricted to those tests authorized by this policy to detect drug abuse. They shall not be used for other purposes, such as the analyses of physiological states or diseases (e.g., pregnancy, AIDS or cancer therapy).
Test Methodology. The substitution method according to ISO 11451-1, shall be used to establish the test field conditions.
Test Methodology. Product Testing Set-up, Methodology, and Documentation: The testing and measurement methods below reference published specifications from the Video Electronics Standards Association (VESA) Display Metrology Committee and the International Electrotechnical Commission (IEC), and supplement those guidelines where necessary with methods developed in cooperation with the computer monitor industry. Manufacturers are required to perform tests and self-certify those product models that meet the ENERGY STAR guidelines. Families of computer monitor models that are built on the same chassis and are identical in every respect but housing and color may be qualified through submission of test data for a single, representative model. Likewise, models that are unchanged or that differ only in finish from those sold in a previous year may remain qualified without the submission of new test data, assuming the specification remains unchanged. The power requirement shall be measured from the outlet or power source to the product under test. The average true power consumption of the computer monitor shall be measured during the On Mode/Active Power, the Sleep Mode/Low Power, and the Off Mode/Standby Power. When performing measurements to self-certify a product model, the product being tested must initially be in the same condition (e.g., configuration and settings) as when shipped to the customer, unless adjustments need to be made pursuant to instructions below. To ensure a consistent means for measuring the power consumption of electronics products, the following protocol must be followed, which has three main components: Product Testing Set-up and Conditions: Outlined below in Sections 1(a) through (h) are the ambient test conditions and measurement protocols that must be respected when performing power measurements.
Test Methodology. UAT shall be conducted by end users, subject matter experts, and/or the County’s body camera project team. Users shall execute all test procedures referenced in section 3. Users may also perform additional tests not detailed in the plan but remain relevant and within the scope of the project, as mutually agreed upon by TASER and the Agency. Such additional test procedures (if any) shall be attached to this document as an Appendix.
Test Methodology. The testing methodology to be used for both “reasonable suspicion” and random testing shall be the same as described herein and will be based on a laboratory examination of a bodily fluid (e.g., urine, oral fluid, etc.) specimen or breath test. Specimen collection and laboratory examination are described in Section IV, Specimen Collection and Section V, Laboratory Analysis. Laboratory analyses of urine specimens shall be restricted to those tests authorized by this policy to detect drug abuse. They shall not be used for other purposes, such as the analyses of physiological states or diseases (e.g., pregnancy, AIDS or cancer therapy).
Test Methodology. The testing methodology will be based on a laboratory examination of a urine specimen and shall meet all analytical, quality assurance and quality control standards as set by NIDA/SAMHSA. Laboratory analyses of urine specimens shall be restricted to those tests authorized by this agreement to detect drug abuse. They shall not be used for other purposes, such as the analyses of physiological states or diseases (e.g., pregnancy, AIDS).