Laboratory Requirements. 1. Urine Testing In testing urine samples, the testing laboratory shall test specifically for those drugs and classes of drugs and adulterants employing the test methodologies and cutoff levels covered in the DOT Regulations 49 CFR, Part 40.
Laboratory Requirements a) The CQAF’s testing laboratory identified in the Construction Quality Management Plan (CQMP) shall conduct Developer’s quality acceptance tests and shall comply with the requirements of the AASHTO Accreditation Program (AAP) or other appropriate accreditation acceptable to TxDOT for the pertinent test. Developer shall transmit to TxDOT a copy of AAP accreditation certificate(s) upon receipt by the testing laboratory.
Laboratory Requirements. The Navajo Nation adopts the certified laboratory lists maintained by the USEPA or any state with primacy over that state's drinking water program, as they may be amended from time to time. Public water system owners or operators are required to use a certified laboratory from such lists in contracting for laboratory services. The Director may maintain a service contract with one or more certified laboratories to meet this requirement.
Laboratory Requirements. Intractable pain patients require regular laboratory testing (e.g. analysis of saliva, urine, and/or blood). Patients who do not obtain or do not consent to the required testing may be discharged from the program.
Laboratory Requirements. NO CHANGE F. Non-Suspicion-Based Post-Accident Testing NO CHANGE G. Substance Abuse Professional (SAP) NO CHANGE
Laboratory Requirements. All testing will be conducted by third party, independent laboratories unless otherwise mutually agreed by the Parties. The Parties shall designate one or more laboratory(ies) for testing and mutually develop protocols and other technical requirements for sampling and testing. Pre-approved laboratories include Soil Control Laboratories of Watsonville, California and Midwest Laboratories of Omaha, Nebraska. Laboratory testing is at Owner’s expense. Bulk Density Determination for Soil Amendments & Other Materials (compost, solid manures, biosolids, SSO, etc) Materials
Laboratory Requirements. This section specifies the minimum requirements that must be met to provide data of known and usable quality to RWQCB and USEPA in support of the SGV and SFV investigations. These requirements include a laboratory certification/ PE program, QA/ QC documentation, and data validation. Laboratories selected for the project must be capable of providing the appropriate analytical detection limits, reporting limits, required turnaround times, project quality control , and data deliverables required by this QAPP. The laboratory m ust have the demonstrated ability to analyze samples of similar type, quantity, and concentrations to be subcontracted. Prior to work on a project, the laboratory will provide: MDL studies and laboratory -specific quantitation limits at or below the project -specific screening levels; soils sample re sults will be reported on a dry -weight basis. Minimum QA/ QC criteria for initial and continuing calibration and interference check samples. Minimum QA/ QC criteria for surrogate recoveries, laboratory control sampl es, blanks, MS/ MSDs indicating that the methods selected for performing analysis can be met. The analytical laboratories selected to perform samples analysis shall be certified by the SWRCB through the Environmental Laboratory Accreditation Program (ELAP) for each required method. Data whose quality do not meet the requirements of this document, regardless of laboratory cer tification, shall be excluded. These requirements apply to onsite mobile laboratories as well as offsite, fixed laboratories. Mobile lab oratories are expected to adhere to all of the specifications of the RWQCB quality program as presented in this QAPP and associated guidance documents. Method modifications or other deviations from QAPP requirements required due to the specialized nature of field laboratory operations must be detailed in the facility -specific work plan. Mobile laboratories must be certified though the Environmental Laboratory Accreditation Program. The use of mobile laboratories shal l be documented in the facility -specific work plan. The mobile laboratory quality assurance plan should be provided as part of the facility -specific work plan. The facility -specific work plan should include a plan for collection of split samples for analysis by a fixed laboratory at a frequency o f 10 percent of the total number of sample s collected when a mobile laboratory is employed . In addition, facilities that use mobile laboratories, RWQCB wil...
Laboratory Requirements. The sampling plan should name the laboratory to be utilized to analyze samples and their qualifications; (H) SAMPLE HANDLING: Sample preservation and other handling practices should be described; Health and Safety Plan: The Sampling Plan shall also include a description of the Health and Safety Plan of the Consultant addressing suspected hazards and risks; levels of protective clothing or equipment to be worn; decontamination procedures; and documentation of the appropriate health and safety training given to the sampling crew; (I)
Laboratory Requirements. The laboratory shall possess the appropriate well-documented procedures, instrumentation, and trained personnel to perform the necessary analyses included in the scope of the project in the frame of required time schedule. The laboratory shall possess a radioactive materials handling license for the samples to be analyzed and will be able to prove experience in performing the same or similar analyses. It shall also fulfill requirements for laboratories which are qualified to provide analyses of non- active waste due to their classification [24]. It shall have an active and fully documented QA program in place, complying with the objectives determined by the DQO process. The QA program should include laboratory organizational structure; personnel qualifications; written standard operating procedures and instructions; inter - and intralaboratory performance analyses; design control to define the flow of samples through the laboratory; a corrective action plan; and an internal audit program. Additionally, the laboratory shall count on the capacity to provide the results on time.
Laboratory Requirements
