Authorized laboratory definition

Authorized laboratory means a laboratory that is:
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Authorized laboratory means any laboratory accredited by an authorized accreditation body in accordance with a standard based on “ISO/IEC/EN 17025: General Requirements for Competence of Calibration and Testing Laboratories”;
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Authorized laboratory means a laboratory that meets the requirements of the United States Department of Agriculture, Animal and Plant Health Inspection Service and is thus qualified to perform testing required to determine classification of poultry and to test for avian pathogens.
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Examples of Authorized laboratory in a sentence

  • Copy of Lab test Report which will be carried out from Govt./ Authorized laboratory approved by NABL in Original.

  • Authorized laboratory An authorized laboratory is a laboratory that meets the requirements of §147.52 and is thus qualified to perform assays in accordance with part 147 of this subchapter.

  • Authorized laboratory personnel should review the results before release and evaluate them against internal quality control and, as appropriate, available clinical information and previous test results.

  • Authorized laboratory shall promptly report the results of its analysis to the relevant chief state sanitary doctor or relevant chief state veterinary inspector, or their deputies with the purposes to adopt a decision regarding further disposition of the above object subject to sanitary measures.

  • Authorized laboratory personnel can perform these functions but only without keys or combination access to the safe or cabinet where bulk quantities of controlled substances are stored.

  • Authorized laboratory personnel do not require a DEA background check or screening.

  • Authorized laboratory An authorized laboratory is a laboratory that meets the requirements of §147.52 and is thus qualified to perform the assays in accordance with part 147 of this subchapter.

  • The engineering services currently provided by POE involves the provision of software and fine engineering design work, such as detailed engineering and front end engineering design as requested by client using POE‟s proprietary engineering software.

  • Authorized laboratory customers include all Active Army, Army Reserve, Army National Guard and other Department of Defense (DoD) customers as designated by the AOAP PMO; Redstone Arsenal activities such as the Redstone Technical Test Center (RTTC); Program Executive Offices (PEO); Combat Capabilities Development Command (CCDC); and Security Assistance Management Directorate (SAMD) offices.

  • In the definition of equivalent orequivalent requirements, by adding the words ‘‘or exceed’’ after the words ‘‘equal to’’ and the words ‘‘they are’’ after the words ‘‘with which.’’§ 145.1 Definitions.* * * * *Authorized laboratory.


More Definitions of Authorized laboratory

Authorized laboratory is a dental laboratory that maintains a current professional license and/or accreditation in good standing and that may be designated by a User to receive Content via the Site. "User" is a licensed health care professional whose professional license and/or accreditation is current and in good standing. "Partner" is a licensed health care professional, dental laboratory, dental technician, and/or dental radiologist that may accept Content through the Site. All partners must hold a current license for the Site and maintain in good standing any and all applicable professional licenses or accreditations.
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Authorized laboratory means a National Poultry Improvement Plan (“NPIP”) authorized laboratory that meets the requirements of the 9 CFR part 147.52 and is thus qualified to perform assays in accordance with the 9 CFR part 147 and NPIP Program Standards. Authorized laboratories performing the Avian Influenza RRT-PCR must also meet standards stipulated in 9 CFR part 145.14 (d)(2)(i).
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Authorized laboratory means a legal person carrying out testing of genetically modified organisms and products containing genetically modified organisms;
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Related to Authorized laboratory

  • 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.

  • 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.

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

  • 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.

  • 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:

  • 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.

  • Dental laboratory means a person, firm or corporation

  • Authorized nuclear pharmacist means a pharmacist who:

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

  • 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.

  • Investigational Medicinal Product means the study drug or control material as defined in the Protocol.

  • 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.

  • Good Laboratory Practices or “GLP” means the then-current good laboratory practice standards promulgated or endorsed by the FDA, as defined in U.S. 21 C.F.R. Part 58 (or such other comparable regulatory standards in jurisdictions outside the United States, as they may be updated from time to time).

  • 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.

  • cGMP means current Good Manufacturing Practice as set forth in the United States Federal Food, Drug, and Cosmetic Act, as amended, and includes all rules and regulations promulgated by the FDA thereunder.

  • Participating Certified Clinical Nurse Specialist means a Certified Clinical Nurse Specialist who 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.

  • Manufacturing means all activities related to the manufacture of a Compound, including planning, purchasing, manufacture, processing, compounding, storage, filling, packaging, waste disposal, labeling, leafleting, testing, quality assurance, sample retention, stability testing, release, dispatch and supply, as applicable.

  • Approved clinical trial means a phase I, phase II, phase III, or phase IV clinical trial that is conducted in relation to the prevention, detection, or treatment of cancer or other life-threatening disease or Condition and is described in any of the following:

  • Manufacturing Process means any process for—

  • Analytical x-ray system means a group of components utilizing x-rays to determine the elemental composition or to examine the microstructure of materials.

  • Quality system means documented organizational procedures and policies: internal audits of those policies and procedures: management review and recommendation for quality improvement.”

  • 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;

  • Radiopharmaceutical quality assurance means, but is not limited to, the performance of appropriate chemical, biological, and physical tests on potential radiopharmaceuticals and the interpretation of the resulting data to determine their suitability for use in humans and animals, including internal test assessment, authentication of product history, and the keeping of proper records.

  • Non-Participating Certified Clinical Nurse Specialist means a Certified Clinical Nurse Specialist who does not have 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.

  • Authorized medical physicist means an individual who:

  • 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.