Therapeutic Goods Administration definition

Therapeutic Goods Administration or “TGA” means the Australian regulatory authority, or any successor agency thereto.
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Therapeutic Goods Administration means the unit within the Commonwealth Department of Health and Ageing responsible for administering the Therapeutic Goods Act 1989 (Cth), and the Regulations and Orders made pursuant to it, including evaluation and approval of medical products.
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Therapeutic Goods Administration means the regulatory body known as the Therapeutic Goods Administration (TGA) that is part of the Commonwealth Government Department responsible for the Therapeutic Goods Act 1989 of the Commonwealth; and
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Examples of Therapeutic Goods Administration in a sentence

  • Australian Government, Department of Health, Therapeutic Goods Administration.

  • From his end, Jonathan Ferris concludes that these payments were the payments that he claimed to have found by Sahra FZCO and, according to him, paid directly to Michelle Buttigieg of Buttardi.

  • These generally apply to items that are not covered or restricted by the government’s Pharmaceutical Benefits Scheme (PBS) and approved under the Therapeutic Goods Administration.

  • The Parties shall seek to advance the existing dialogue between the Australian Therapeutic Goods Administration and the U.S. Food and Drug Administration with a view to making innovative medical products more quickly available to their nationals.

  • The regulatory system in Australia will comprise the existing regulators with a legal remit to cover some aspects of GM products (such as imports, food, agricultural and veterinary chemicals): • the Australia New Zealand Food Authority (ANZFA)• the Therapeutic Goods Administration (TGA)• the National Registration Authority for Agricultural and Veterinary Chemicals (NRA)• the National Industrial Chemicals Notification and Assessment Scheme (NICNAS)• the Australian Quarantine and Inspection Service (AQIS).

  • Therapeutic Goods Administration codes of practice, Australian Council of Healthcare Standards, ISO 9000 and Australian Standards.

  • Product development involves lengthy processes and is subject to evaluations by external groups such as the United States Food and Drug Administration (“FDA”) and Australian Therapeutic Goods Administration (“TGA”).

  • It reflects the shared views of the all state and territory Departments of Health, the Therapeutic Goods Administration (TGA), National Health and Medical Research Council (NHMRC) and the Clinical Trials Project Reference Group (CTPRG), of which all of these entities are members.

  • All items offered must be approved by the Australian Therapeutic Goods Administration (TGA), unless exempt.

  • Therapeutic Goods Administration (TGA) - Australian Code of Good Manufacturing Practice for human blood and blood components, human tissues and human cellular therapy products - Version 1.0, April 2013.

Related to Therapeutic Goods Administration

  • Medication administration means the direct application of medications by injection, inhalation, ingestion, or any other means to an individual receiving services by (i) persons legally permitted to administer medications or (ii) the individual at the direction and in the presence of persons legally permitted to administer medications.

  • Self-Administration of Medication means the individual manages and takes his or her own medication, identifies his or her medication and the times and methods of administration, places the medication internally in or externally on his or her own body without staff assistance upon written order of a physician, and safely maintains the medication without supervision.

  • Customs Administration means the competent authority that is responsible under the law of a Party for the administration of customs laws and regulations;

  • Drug means (i) articles or substances recognized in the official United States Pharmacopoeia

  • Self-administration means carrying and taking medication without the intervention of the school nurse, approved through the school district policy and restricted to students with asthma, other potentially life-threatening illnesses or life-threatening allergic reaction.

  • Authorized nuclear pharmacist means a pharmacist who:

  • Therapeutic interchange means an authorized exchange of therapeutic alternate drug products in accordance with a previously established and approved written protocol.

  • international application means an application filed under this Treaty;

  • Therapeutic school means a residential group living facility:

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

  • Claims Administration means the processing of claims made under the Shared Policies, including the reporting of claims to the insurance carriers, management and defense of claims and providing for appropriate releases upon settlement of claims.

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

  • Administration of Medication means the act of placing a medication in or on an individual's body by a staff member who is responsible for the individual's care.

  • 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.

  • Therapeutic diet means meals served that are soft, low-fat, low-sodium or controlled calorie.

  • Therapeutic care means services provided by licensed or certified speech pathologists, Occupational Therapists and Physical Therapists.

  • Veterinarian means a veterinarian authorized by law to practice veterinary medicine in this State.

  • veterinary surgeon means a veterinary surgeon within the meaning of the Veterinary Surgeons Act 1936.

  • Electrostatic application means the application to a substrate of charged atomized paint droplets that are deposited by electrostatic attraction.

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

  • Medical evaluation means the process of assessing an individual's health status that includes a medical history and a physical examination of an individual conducted by a licensed medical practitioner operating within the scope of his license.

  • Pharmaceutical care means the provision of drug therapy and

  • School of cosmetology means an establishment operated for the purpose of teaching cosmetology.

  • Home health aide means an individual employed by a home health agency to provide home health services under the direction of a registered nurse or therapist.

  • Centralized prescription processing means the processing by a pharmacy of a request from another pharmacy to fill or refill a prescription drug order or to perform processing functions such as dispensing, drug utilization review, claims adjudication, refill authorizations, and therapeutic interventions.

  • Mobile Application means a specialized software program downloaded onto a wireless communication device.