DNA Laboratory definition

DNA Laboratory means the laboratory areas located on the 5th, 6th, 7th, and 8th floors of the OCME Forensic Biology Building. See “OCME Forensic Biology Building,” below.
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DNA Laboratory means a laboratory that
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DNA Laboratory means a laboratory that 3-55 performs forensic DNA analysis on samples or specimens derived from 3-56 a human body, physical evidence, or a crime scene. The term 3-57 includes a department crime laboratory facility that conducts 3-58 forensic DNA analysis.
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Examples of DNA Laboratory in a sentence

  • It is mandatory that any and all persons entering the DNA Laboratory be attired in protective wear meeting OCME specifications prior to entering a DNA Laboratory Area.

  • All Contractor personnel and other employees provided by the Contractor are prohibited from making photocopies of or removing anything from the DNA Laboratory or any OCME facility.

  • The Contractor is responsible under the terms of this Contract for informing its employees that they will need to give a sample of their DNA as a condition of employment and service in the DNA Laboratory.

  • All Contractor personnel and other employees provided by the Contractor performing work within a DNA Laboratory Area must be escorted by an OCME employee at all times.

  • Students may apply up to two courses from their major to satisfy Stage 1 and Stage 2 of the Core; only one of these is permitted to fulfill a Stage 1 requirement and only one a Stage 2 requirement.*5.

  • Non-negative moment-fitting quadratures also lead to such scattering, but to a smaller extent.

  • This DNA profile will then be placed in a Quality Control database maintained by the OCME that will be used only to conduct routine contamination screenings for all work performed in the DNA Laboratory.

  • All Contractor personnel and other employees provided by the Contractor to perform services in a DNA Laboratory Area or in an area where biological samples are sent for DNA testing, such as a morgue, pursuant to this Contract are required to submit a DNA sample for testing and placement in a Quality Control database maintained by OCME as described herein.

  • OCME requires that all attorneys who intend to call a criminalist as a witness at trial have a pre-trial meeting here at the OCME DNA Laboratory Building with the assigned analyst.

  • Each quarterly report shall state the total, annual, and quarterly number of qualifying profiles in the Department of Justice DNA Laboratory data bank both from persons and case evidence, and the number of hits and investigations aided, as reported to the National DNA Index System.

Related to DNA 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.

  • 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 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.

  • 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).

  • 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.

  • GLP means the then-current good laboratory practice standards promulgated or endorsed by the FDA as defined in 21 C.F.R. Part 58 or the successor thereto, or comparable regulatory standards in jurisdictions outside of the United States, to the extent such standards are not less stringent than United States standards.

  • Bioassay means the determination of kinds, quantities or concentrations and, in some cases, the locations of radioactive material in the human body, whether by direct measurement, in vivo counting, or by analysis and evaluation of materials excreted or removed from the human body. For purposes of these rules, “radiobioassay” is an equivalent term.

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

  • 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;

  • 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.

  • Clinical means having a significant relationship, whether real or potential, direct or indirect, to the actual rendering or outcome of dental care, the practice of dentistry, or the quality of dental care being rendered to a patient;

  • Therapeutic school means a residential group living facility:

  • Study means the investigation to be conducted in accordance with the Protocol.

  • Step therapy protocol means a protocol or program that establishes the specific

  • 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.

  • scientific research means any activity in the field of natural or applied science for the extension of knowledge;

  • 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.

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

  • 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.