Specimen label definition

Specimen label means a label other than the label attached to a pesticide container that contains the same information as the label attached to the pesticide container labeling.
Specimen label means a label other than the label attached to a pesticide container that contains the same information as the labeling; including an electronic label.
Specimen label means a label other than the label attached to a pesticide container that contains the same

Examples of Specimen label in a sentence

  • Specimen label for Infusion Bag - “double tear off” label Each of the 2 sections of the double label will have identical information as per specimem below.

  • After approval of the pesticide list, the Bidder shall supply to each facility, the Specimen label and MSDS for each pesticide that is actually used at that facility.

  • The chapter deals with analyzing the reasons from two main sources of objective and subjective perspectives.

  • Specimen label images are important for data quality control and specimen images are needed for identification, trait and taxonomic discovery.

  • Specimen label templates provided by the SDMC include this information.Accountability for the samples must be maintained, with requirements for signatures of each individual who handled the specimen.

  • Specimen label is for demonstration purposes only, for product application consult product packaged label.

  • Figure 4.4 Load-deflection and crack pattern graph of Square panel-(0.9%) Table 4.5 Properties of Square Panel- (0.9%) Specimen label For 0.9% samples, sample one absorbed the highest energy and achieved the highest peak load.

  • Specimen label for the REPARIXIN Vial STUDY REP0112Sponsor Dompé s.p.a.; Via Campo di Pile, L’Aquila – Italy Phone: + 39 346 8745908 REPARIXININVESTIGATOR: CONTAINS: 250 mL REPARIXIN (33 mg/mL) CONCENTRATE FOR SOLUTION FOR I.V. INFUSIONBATCH No.EXPIRY DATE mm/yyyyDO NOT STORE AT >30°C (86°F)DIRECTIONS: Transfer into an INFUSION BAG the content of the vial + 500 mL of 0.9% NaCl, according to procedures detailed in the “Instructions to the Pharmacy”.

  • Specimen label Figure 4.3 Load-deflection and crack pattern graph of Square panel-(0.6%) Table 4.4 Properties of Square Panel- (0.6%) For 0.6% square panels, there is no difference in the elastic zone.

  • Specimen label Figure 4.1 Load-deflection garph of control Square panel-(0.0%) Table 4.2. Properties of the square panel- control Specimen label Figure 4.2 Load-deflection and crack pattern graph of Square panel-(0.3%) Table 4.3 Properties of Square Panel- (0.3%) For the square plates with 0.3% fibers in volume contents, a noticeable decrease has obtained after the first crack in the load-carrying capacity followed by a strain hardening.

Related to Specimen label

  • Specimen means tissue, hair, or a product of the human body capable of revealing the presence of drugs or their metabolites, as approved by the United States Food and Drug Administration or the Agency for Health Care Administration.

  • Product Labeling means, with respect to a Licensed Product in a country or other jurisdiction in the Territory, (a) the Regulatory Authority‑approved full prescribing information for such Licensed Product for such country or other jurisdiction, including any required patient information, and (b) all labels and other written, printed, or graphic matter upon a container, wrapper, or any package insert utilized with or for such Licensed Product in such country or other jurisdiction.

  • Authorized Persons means Contractor’s employees, officers, partners, Subcontractors or other agents of Contractor who need to access State Data to enable Contractor to perform its responsibilities under Contract.

  • Sample means urine, blood, breath, saliva, or hair.

  • Tobacco product manufacturer means an entity that after the date of enactment of this Act directly (and not exclusively through any affiliate):

  • Authorized pharmacist means an Iowa-licensed pharmacist whose license is in good standing and who meets the drug therapy management criteria defined in this rule.

  • Marketing Authorization Application or “MAA” means an application for Regulatory Approval (but excluding Pricing Approval) in any particular jurisdiction other than the U.S.

  • Authorized Personnel means the employees of the Licensee and personnel from third parties who work on behalf of the Licensee under a contract (which shall include confidentiality clause) entered into and between the Licensee and the third party.

  • Labeling means all labels and other written, printed, or graphic matter on an article or any of its

  • Split Specimen means a part of the oral fluid specimen in drug testing that is retained unopened for a confirmation test (if required) or in the event that the employee requests that it be tested following a verified positive test of the primary specimen or a verified Adulterated or Substituted Specimen test result.

  • Contract Manufacturer means a company that produces goods under contract for another company under the label or brand name of that company.

  • Direction-indicator lamp means the lamp used to indicate to other road-users that the driver intends to change direction to the right or to the left;

  • Goods Specification means any specification for the Goods, including any related plans and drawings that is set out in the Purchase Order or otherwise agreed in writing by the Customer and the Supplier;

  • Engine Manufacturer means CFM International, Inc.

  • Functional Specifications means the descriptions of features and functions of the Application as expressly set forth in Quote.

  • API means the American Petroleum Institute.

  • Authorized prescriber means a physician, dentist, advanced practice registered nurse or physician assistant;

  • Product means any deliverable under the Contract, which may include commodities, services, technology or software.

  • Brand Name Specification means a specification limited to one or more items by manufacturers’ names or catalogue number.

  • Product Manufacturer means the entity that assembles the component parts to manufacture the final Product;

  • Product Specifications means the specifications, features and/or terms of any "Contract" (as defined in the LME Rules) listed for trading on the LME, as described in the LME Rules;

  • Manufacturer means the person or body who is responsible to the approval authority for all aspects of the type approval process and for ensuring conformity of production. It is not essential that the person or body is directly involved in all stage of the construction of the vehicle, system, component or separate technical unit which is the subject of the approval process.

  • Finished Product means a cannabis product in its final form to be sold at a retail premises.

  • Adulterated Specimen means a specimen that contains a substance that is not expected to be present in oral fluid, or contains a substance expected to be present but is at a concentration so high that it is not consistent with oral fluid.

  • Feed ingredient means each of the constituent materials making up a commercial feed.

  • Tobacco product means any substance containing tobacco leaf, including but not limited to, cigarettes, cigars, pipe tobacco, hookah tobacco, snuff, chewing tobacco, dipping tobacco, bidis, blunts, clove cigarettes, or any other preparation of tobacco; and any product or formulation of matter containing biologically active amounts of nicotine that is manufactured, sold, offered for sale, or otherwise distributed with the expectation that the product or matter will be introduced into the human body by inhalation; but does not include any cessation product specifically approved by the U.S. Food and Drug Administration for use in treating nicotine or tobacco dependence.