Test Methodology. 5.1.1. The substitution method according to ISO 11451-1, shall be used to establish the test field conditions.
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. General If the Owner is in doubt about the compliance of one or more WTG with the WNEL, the Owner has the right to have the noise emission level verified at any WTG at his own cost by a test laboratory selected from the list set forth in 5.4 of this Part J-2-C. The Supplier has the right to participate during the measurement. Within reasonably limits, the Supplier has the right to reject: the complete report, parts of the report, limitation of the confidence interval K and further measurements by the chosen testing laboratory under the purpose of this Sound power level Warranty. The Parties will in good faith collaborate in the discussions, agreements and solutions that can be required during the development of the activities described in this Part J-2-C, aiming the successful conclusion of the activities in this Part J-2-C. Should reasonable doubts about the quality of the measurement, procedures and/or the testing laboratory exist, the Supplier shall notify the Owner as soon as possible as this becomes apparent. The Supplier will provide the required support during the noise level test in those activities which require the intervention on the TWTs, at no cost. The measurement shall be carried out in accordance with [Ref.1].
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. 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 guide- lines. Families of computer monitor models that are built on the same chassis and are identical in every respect but housing and colour 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 with- out 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. 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).
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.
