Single laboratory definition

Single laboratory means an individual laboratory facility or multiple laboratory facilities located on contiguous grounds and owned by the same person.
Sample 1Sample 2Sample 3
Single laboratory means an individual laboratory facility or multiple laboratory
Sample 1
Single laboratory means an individual laboratory facil- ity or multiple laboratory facilities located on contiguous grounds and having the same owner.
Sample 1

Examples of Single laboratory in a sentence

  • The envelope or package must be clearly labeled with the name and number of RFA-17-0003 as indicated on the cover page.

  • Single laboratory accuracy and precision data from both fortified reagent water and fortified drinking water matrices are presented in Tables 4 and 5, respectively.

  • Single laboratory accuracy, precision and MDL data for method analytes are provided in Tables 1-1 through 1-2 in Appendix 1.

  • ACCURACY AND MDLs-- Single laboratory accuracy and precision data from both fortified reagent water and fortified matrices using hot, splitless injection are presented in Tables 4 and 5.

  • Single laboratory precision and accuracy data are presented in Tables 4-6.

  • Single laboratory accuracy, precision and MDL data for method analytes are provided in Tables 1-1 through 1- 2 in Appendix 1.

  • ACCURACY AND DLs-- Single laboratory accuracy and precision data from both fortified reagent water and fortified matrices are presented in Tables 3-20.

  • Single laboratory precision for the Mulinia lateralis larvae test and the amphipod tests using Ampelisca and Hyalella has not been previously determined, but will be assessed prior to and during the conduct of the Near Coastal Demonstration Project to establish acceptable precision levels in the future.

  • AK updated the group regarding changes since 20th of August 2015 on the following: New CEO now in place Continuing on trajectory for setting up the 2 x hubs Setting up Single laboratory system with better standardised information across the board, apart from Cambridge Working on batch reporting HB asked if TPP are working with ENHT regarding microbiology in particular.

  • Therefore, the enforcement policies in this guidance do not apply to DTC tests, and FDA’s usual enforcement policies apply to DTC tests.5 Single laboratory refers to a facility with a single CLIA certificate as described in 42 CFR 493.43(a)-(b).

Related to Single laboratory

  • Testing laboratory means a laboratory, facility, or entity in the state that offers or performs tests of cannabis or cannabis products and that is both of the following:

  • Clinical laboratory means a facility for the microbiological, serological, chemical, hematological, radiobioassay, cytological, immunohematological, pathological, or other examination of materials derived from the human body for the purpose of providing information for the diagnosis, prevention, or treatment of a disease or assessment of a medical condition.

  • Approved laboratory means a laboratory that is listed in the national conference of interstate milk shipments list of sanitation compliance and enforcement ratings distributed by the United States food and drug administration and as approved by the director.

  • Dental laboratory means a person, firm or corporation

  • Participating Clinical Laboratory means a Clinical Laboratory which has a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan to provide services to you at the time services are rendered.

  • Independent testing laboratory means an independent organization, accepted by the Contracting Officer, engaged to perform specific inspections or tests of the work, either at the site or elsewhere, and report the results of these inspections or tests.

  • Laboratory or “LANL” means the geographical location of Los Alamos National Laboratory, a federally funded research and development center owned by the DOE / NNSA.

  • Good Laboratory Practice or “GLP” means the applicable then-current standards for laboratory activities for pharmaceuticals (including biologicals) or vaccines, as applicable, as set forth in the Act and any regulations or guidance documents promulgated thereunder, as amended from time to time, together with any similar standards of good laboratory practice as are required by any Regulatory Authority having jurisdiction over the applicable activity.

  • Clinical nurse specialist means a registered nurse with relevant post-basic qualifications and 12 months’ experience working in the clinical area of his/her specified post-basic qualification, or a minimum of four years’ post-basic registration experience, including three years’ experience in the relevant specialist field and who satisfies the local criteria.

  • Non-Participating Clinical Laboratory means a Clinical Laboratory which does not have a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan provide services to you at the time services are rendered.

  • Certified laboratory means a laboratory that is on an approved list issued by us.

  • Good Laboratory Practices or “GLP” means the then-current Good Laboratory Practice (or similar standards) for the performance of laboratory activities for pharmaceutical products as are required by applicable Regulatory Authorities or Applicable Law. In the United States, Good Laboratory Practices are established through FDA regulations (including 21 C.F.R. Part 58), FDA guidance, FDA current review and inspection standards and current industry standards.

  • Cosmetology means the art or practice of embellishment, cleansing, beautification, and styling of hair, wigs, postiches, face, body, or nails.

  • Community mental health program means all mental health

  • Design Criteria Professional means a firm who holds a current certificate of registration under Chapter 481 of the Florida Statutes, to practice architecture or landscape architecture, or a firm who holds a current certificate as a registered engineer under Chapter 471 of the Florida Statutes, to practice engineering, and who is employed by or under contract to the District to provide professional architect services, landscape architect services, or engineering services in connection with the preparation of the Design Criteria Package.

  • accredited laboratory means an analytical facility accredited by the Standards Council of Canada (SCC), or accredited by another accrediting agency recognized by Manitoba Conservation and Climate to be equivalent to the SCC, or be able to demonstrate, upon request, that it has the quality assurance/quality control (QA/QC) procedures in place equivalent to accreditation based on the international standard ISO/IEC 17025, or otherwise approved by the Director;

  • Cluster development means a contiguous cluster or

  • Screening means the evaluation process used to identify an individual's ability to perform activities of daily living and address health and safety concerns.

  • GMP means the amount proposed by Contractor and accepted by Owner as the maximum cost to Owner for construction of the Project in accordance with this Agreement. The GMP includes Contractor’s Construction Phase Fee, the General Conditions Cost, the Cost of the Work, and Contractor’s Contingency amount.

  • Testing means that element of inspection that determines the properties or elements, including functional operation of materials, equipment, or their components, by the application of established scientific principles and procedures.

  • Prescription drug means any drug required by federal law or regulation to be dispensed only

  • Scaling as used herein, involves:

  • Validation as used in WAC 222-20-016, means the department's agreement that a small forest landowner has correctly identified and classified resources, and satisfactorily completed a roads assessment for the geographic area described in Step 1 of a long-term application.

  • Collaborative drug therapy management means participation by an authorized pharmacist and a physician in the management of drug therapy pursuant to a written community practice protocol or a written hospital practice protocol.

  • Assay means a laboratory analysis of Crude Petroleum to include the following: A.P.I. Gravity, Reid vapor pressure, composition, pour point, water and sediment content, sulfur content, viscosity, distillation, hydrogen sulfide, flash/boiling point and other characteristics as may be required by Carrier.

  • Protocols means written directions and orders, consistent with the department’s standard of care, that are to be followed by an emergency medical care provider in emergency and nonemergency situations. Protocols must be approved by the service program’s medical director and address the care of both adult and pediatric patients.