Agency for Medicinal Products and Medical Devices definition

Agency for Medicinal Products and Medical Devices means a legal person established pursuant to the Act on Medicinal Products and Medical Devices (Official Gazette 121/03), hereinafter „the Agency“, whose scope of activities in the field of medicinal products and homeopathic medicinal products is governed by this Act.
Agency for Medicinal Products and Medical Devices means a legal person with public authorities established pursuant to the Act on Medicinal Products and Medical Devices (Official Gazette No. 121/03), hereinafter referred to as the Agency, the scope of which in the area of medicinal products and medical devices is defined by this Act,

Examples of Agency for Medicinal Products and Medical Devices in a sentence

  • Reason why uses advised against:The product is intended for use only as an in vitro diagnostic medical device, registered at the Agency for Medicinal Products and Medical Devices and there is no reason to use it for other purposes.1.3Details of the supplier of the safety data sheet Supplier:BioGnost Ltd.

  • Reason why uses advised against:The product is intended for use only as an in vitro diagnostic medical device, registered at the Agency for Medicinal Products and Medical Devices and there is no reason to use it for other purposes1.3.Details of the supplier of the safety data sheet Supplier:BioGnost Ltd.

  • Reason why uses advised against:The product is intended for use only as an in vitro diagnostic medical device, registered at the Agency for Medicinal Products and Medical Devices and there is no reason to use it for other purposes.1.3.Details of the supplier of the safety data sheet Supplier:BioGnost Ltd.

  • Agency for Medicinal Products and Medical Devices of Croatia [Internet].

  • Reason why uses advised against:The product is intended for use only as an in vitro diagnostic medical device listed in the Registry of medical devices at the Agency for Medicinal Products and Medical Devices and there is no reason to use it for other purposes1.3.Details of the supplier of the safety data sheet Supplier:BioGnost Ltd.

  • The medicinal product is considered a product that has been granted a marketing authorization in the Republic of Serbia and a product that has not been granted a marketing authorization in the Republic of Serbia, which is imported on the basis of the approval of the Agency for Medicinal Products and Medical Devices of Serbia, in accordance with the law regulating the field of drugs.

  • Accessed 10 August 2020.[3] Agency for Medicinal Products and Medical Devices of the Republic of Slovenia (JAZMP).

  • According to the Agency for Medicinal Products and Medical Devices (HALMED), the rate of consumption showed a slow and constant growth between 2010 and 2014 [7].The growth was approximately 3% per year in DDD/TID, while financial expenditure remained stable with, on average, a minimum increase in price of 0.3% per year [7].

  • In 2021, 3 inspections in PC Pharmaceuticals were performed by our national Competent Authority MALMED (Macedonian Agency for Medicinal Products and Medical Devices) for re- newal of the Certificate of GMP compliance for the production site on Blvd.

  • Allowing expeditious patient transfers for the duration of the emergency will ensure patients who need acute care have access.

Related to Agency for Medicinal Products and Medical Devices

  • Consumables and medical devices means (consumables) items that require regular replacement (e.g. batteries) to keep a medical device (such as a hearing aid) operational. Many medical devices require consumables.

  • medicinal product means any substance or combination of substances presented for treating or preventing disease in human beings or animals and any substance or combination of substances which may be administered to human beings or animals with a view to making a medical diagnosis or to restoring, correcting or modifying physiological functions in humans or in animals;

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

  • Centers for Medicare and Medicaid Services or “CMS” means the federal office under the Secretary of the United States Department of Health and Human Services, responsible for the Medicare and Medicaid programs.

  • Marijuana products means concentrated marijuana products and marijuana products that are comprised of marijuana and other ingredients and are intended for use or consumption, such as, but not limited to, edible products, ointments, and tinctures.

  • Tobacco products means cigars, cigarettes, cheroots, stogies, periques, granulated, plug cut, crimp cut, ready rubbed, and other smoking tobacco, snuff, snuff flour, moist snuff, cavendish, ping and twist tobacco, fine-cut and other chewing tobaccos, shorts, refuse scraps, clippings, cuttings and sweepings of tobacco, and other kinds and forms of tobacco, prepared in such manner as to be suitable for chewing or smoking in a pipe or otherwise, or both for chewing and smoking.

  • in vitro diagnostic medical device means any medical device which is a reagent, reagent product, calibrator, control material, kit, instrument, apparatus, equipment, software or system, whether used alone or in combination, intended by the manufacturer to be used in vitro for the examination of specimens, including blood and tissue donations, derived from the human body, solely or principally for the purpose of providing information:

  • 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.

  • the Products means all products and associated documentation to be supplied under this Contract;

  • Medical marijuana product means a product that contains cannabinoids that have been extracted from plant material or the resin therefrom by physical or chemical means and is intended for administration to a licensed patient, including but not limited to concentrates, oils, tinctures, edibles, pills, topical forms, gels, creams, and other derivative forms, except that this term does not include live plant forms.

  • Red Hat Products means Software, Services, Subscriptions and other Red Hat branded offerings made available by Red Hat.

  • Nuclear medicine technologist means an individual who holds a current certification with the American Registry of Radiological Technologists or the Nuclear Medicine Technology Certification Board.

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

  • Pharmaceutical Product shall have the meaning ascribed to such term in Section 3.1(hh).

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

  • Civil Aeronautical Product means any civil aircraft, aircraft engine, or propeller or subassembly, appliance, material, part, or component to be installed thereon.

  • Products and Services means the products and/or services to be sold by Vendor hereunder as identified and described on Attachment A hereto and incorporated herein, as may be updated from time to time by Vendor to reflect products and/or services offered by Vendor generally to its customers.

  • Manufacturing Services means the manufacturing, quality control, quality assurance, stability testing, packaging, and related services, set forth in this Agreement, required to manufacture Product or Products from Active Materials and Components;

  • Pharmacist services means products, goods, and services, or any combination of products, goods, and services, provided as a part of the practice of pharmacy.

  • Marijuana product means marijuana as defined in 50-32-101 and marijuana-infused products

  • 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.

  • Marijuana wholesaler means a person who purchases marijuana items in this state for resale to a person other than a consumer.

  • medical device means any instrument, apparatus, appliance, software, implant, reagent, material or other article intended by the manufacturer to be used, alone or in combination, for human beings for one or more of the following specific medical purposes:

  • Cannabis wholesaler means any licensed person or entity that purchases or otherwise obtains, stores, sells or otherwise transfers, and may transport, cannabis items for the purpose of resale or other transfer to either another cannabis wholesaler or to a cannabis retailer, but not to consumers.

  • Radiopharmaceutical service means, but is not limited to, the procurement, storage, handling preparation, labeling, quality assurance testing, dispensing, delivery, recordkeeping, and disposal of radiopharmaceuticals and other drugs.

  • Hemp products means all products made from industrial hemp,