Blood components definition

Blood components means that part of blood separated by physical or mechanical means.
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Blood components means therapeutic components that have been manufactured from blood (including red cells, white cells, stem cells, platelets and plasma), except for products derived through fractionation of plasma.
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Blood components means the therapeutic constituents of blood (e.g. red cells, white cells, platelets, plasma) that can be prepared by various methods.
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Examples of Blood components in a sentence

  • The whole Human Blood and Blood components should be screened for all routine and special investigations including Blood grouping, Typing, Cross Matching and other standard as well as specialized tests for HIV, Hepatitis, etc.

  • Services not identified by a revenue code should be placed under subcategory “General Classification.”  Bed scales Blood components (administration of blood is covered.

  • The reelection proposal of Statutory Board Members shall take into account their good performance during the period and their experience for the function, as per theresults of the periodic evaluation process, under the terms of the Novo Mercado Regulation.

  • Blood components produced during Phase 1 may be used therapeutically where they comply with appropriate release criteria.

  • Blood components are sometimes transferred between hospitals either with a patient, or as an efficient use of blood stocks.

  • Preparation of Blood components shall be carried out only under a closed system using single, double, triple or quadruple plastic bags except for preparation of Red Blood Cells Concentrates, where single bags may be used with transfer bags.

  • Blood components: Requisition form, Issue form and Consumption report should be enclosed.

  • These guidelines are intended to be used in conjunction with other established GMP guidelines to provide guidance on the requirements needed to license Blood Facilities (including apheresis facilities) and list Blood components and blood products.

  • Blood components and derivatives, and synthetic blood components and products that are classified as prescription drugs.

  • The following Blood components can be requested, some must be discussed with a Haematology clinician prior to requesting.


More Definitions of Blood components

Blood components means those preparations separated from a single donation of whole blood, or collected by apheresis, intended for direct use in transfusion, including but not limited to plasma, fresh frozen plasma, red blood cells, washed red blood cells, leukocyte-reduced red blood cells, platelets, granulocytes and cryoprecipitate.
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Blood components means those preparations that are separated from whole blood and are intended for use as final products for therapeutic purposes, for further manufacturing, or as products used for in vitro testing.
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Related to Blood components

  • Blood component means that part of blood separated by physical or mechanical means.

  • Structural components means liners, leachate collection systems, final covers, run-on/run-off systems, and any other component used in the construction and operation of the MSWLF that is necessary for protection of human health and the environment.

  • Components means articles, materials, and supplies incorporated directly into end products at any level of manufacture, fabrication, or assembly by the Contractor or any subcontractor.

  • Removed Components means components of the Project or portions thereof which the Company or any Sponsor Affiliate in its sole discretion, elects to remove from the Project pursuant to Section 4.04 hereof or as a result of any Condemnation Event.

  • Manufactured or “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.

  • Certified components means components of X-ray systems which are subject to regulations promulgated under Public Law 90-602, the “Radiation Control for Health and Safety Act of 1968,” the Food and Drug Administration.

  • Drug Substance means an active ingredient that is intended to furnish pharmacological activity or other direct effect in the diagnosis, cure, mitigation, treatment, or prevention of disease or to affect the structure or any function of the human body, but does not include intermediates used in the synthesis of such ingredient.

  • Tooling means tooling inventory, including but not limited to dies, molds, tooling, casting patterns, gauges, jigs, racks and stands for engines, cowls, radome and wheels, aircraft jacks, test benches, test equipment, lathes, welders, grinders, presses, punches and hoists and other similar items (whether or not completed or fixed or handheld).

  • Products means information resources technologies that are, or are related to, EIR.

  • Third Party Components means software and interfaces, licensed by RIM from a third party for incorporation into a RIM software product, or for incorporation into firmware in the case of RIM hardware products, and distributed as an integral part of that RIM product under a RIM brand, but shall not include Third Party Software.

  • Remanufactured means factory rebuilt to original specifications.

  • Appliances means and include electrical, mechanical and electronic appliances such as refrigerator, television, DVD player, videocassette recorder/player, washing machine, microwave oven, music system, personal computer, laptops and air-conditioner contained or fixed in the Insured’s home for domestic use.

  • Remanufacturing means the activity of overhauling, retrofitting, fabricating, or repairing a product or its component parts for ultimate sale at retail.

  • Consumables means where the context permits, Digital Print Consumables, Inkjet Printing System Consumables and Prepress Consumables.

  • 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.

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

  • Manufacturing Site means a location where a manufacturing

  • Food-chain crops means tobacco, crops grown for human consumption, and crops grown for feed for animals whose products are consumed by humans.

  • Raw Materials means all raw materials, supplies, components and packaging necessary to manufacture and ship the Product in accordance with the Specifications, as provided in Exhibit A, but not including the API.

  • Finished Products means any one or more of the following petroleum oils, or a mixture or combination of these oils, to be used without further processing except blending by mechanical means:

  • Fluoroscopic imaging assembly means a subsystem in which X-ray photons produce a visual image. It includes the image receptor(s) such as the image intensifier and spot-film device, electrical interlocks, if any, and structural material providing linkage between the image receptor and diagnostic source assembly.

  • Biological agent shall mean any pathogenic (disease producing) micro-organism(s) and/or biologically produced toxin(s) (including genetically modified organisms and chemically synthesized toxins) which cause illness and/or death in humans, animals or plants.

  • Animal means any nonhuman animate being endowed with the power of voluntary action.

  • Food-contact surface means those surfaces of equipment and utensils with which food normally comes in contact, and those surfaces from which food may drain, drip, or splash back onto surfaces normally in contact with food.