Pharmaceutical Society of Ireland definition

Pharmaceutical Society of Ireland means the body constituted in accordance with section 4 of the Pharmacy Act (Ireland) 1875;
Pharmaceutical Society of Ireland means the 35

Examples of Pharmaceutical Society of Ireland in a sentence

  • This can only be achieved in conjunction with the local hospital pathology service.3. Pharmacies providing NPT services should follow the Guidance on the Provision of Testing Services in Pharmacies from the Pharmaceutical Society of Ireland, and should be aiming for ISO 15189/22870 accreditation as an ultimate goal.

  • Pharmaceutical practice within the prison system will adhere to practice guidelines issued by the Pharmaceutical Society of Ireland.

  • The B.Sc. (Pharm.) course is accredited by the Pharmaceutical Society of Ireland and is also recognised for "free movement" purposes under the various European Union Directives on Pharmacy which lay down the subjects to be studied.

  • Dissolution of old and establishment and membership of new Pharmaceutical Society of Ireland.

  • Through consultation with the CCP Clinical Lead, CCP Clinical Advisory Group, National Health and Social Care Professions (HSCP) Office, Pharmaceutical Society of Ireland, Irish Nutrition and Dietetic Institute, Irish Society for Clinical Nutrition and Metabolism and the Irish Association of Speech and Language Therapists, the document was completed.

  • This can only be achieved in conjunction with the local hospital pathology service.3. Pharmacies providing NPT services should follow the Guidance on the Provision of Testing Services in Pharmacies7 from the Pharmaceutical Society of Ireland (updated October 2019), and should be aiming for ISO 15189/22870 accreditation as an ultimate goal.4. The date of application of the new IVDR is May 2022.

  • Editorial Notes: E1 Registrar of Pharmaceutical Society of Ireland prescribed to be recipient of disclosures of relevant wrongdoings relating to the regulation of pharmacists and pharmacies including the Society’s responsibility for supervising compliance with Act (24.09.2020) by Protected Disclosures Act 2014 (Disclosure to Prescribed Persons) Order 2020 (S.I. No. 339 of 2014), art.

  • These guidelines have been approved by the Pharmaceutical Society of Ireland (PSI), the Health Service Executive (HSE), the Faculty of Pathology (RCPI), the Association of Clinical Biochemists in Ireland (ACBI), the Academy of Medical Laboratory Science (AMLS) and the regulatory agency for medical devices in Ireland, the Irish Medicines Board (IMB).

  • Pursuant to Section 7(1)(d) of the Pharmacy Act 2007, the Pharmaceutical Society of Ireland (“ PSI”) is required to ensure that pharmacists undertake appropriate continuing professional development, including the acquisition of specialisation.

  • These Rules may be cited as the Pharmaceutical Society of Ireland (Registration) Rules 2008.

Related to Pharmaceutical Society of Ireland

  • 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.

  • Pharmaceutical means a drug intended for use in the diagnosis, cure, mitigation, treatment, therapy, or prevention of disease in humans or animals.

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

  • Radiopharmaceutical means any drug that exhibits spontaneous disintegration of unstable nuclei with the emission of nuclear particles or photons and includes any non-radioactive reagent kit or radionuclide generator that is intended to be used in the preparation of any such substance, but does not include drugs such as carbon-containing compounds or potassium-containing salts that include trace quantities of naturally occurring radionuclides. The term also includes any biological product that is labeled with a radionuclide or intended solely to be labeled with a radionuclide.

  • Pharmaceutical care means the provision of drug therapy and

  • 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.

  • Active Pharmaceutical Ingredient or “API” means the active pharmaceutical substance of the Drug in bulk form prior to incorporation into the Product.

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

  • Practice of medicine or osteopathic medicine means the prevention, diagnosis and treatment of

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

  • Biological safety cabinet means a containment unit suitable for the preparation of low to moderate risk agents where there is a need for protection of the product, personnel, and environment, according to National Sanitation Foundation (NSF) Standard 49.

  • Medical management technique means a practice which is used to control the cost or utilization of health care services or prescription drug use. The term includes, without limitation, the use of step therapy, prior authorization or categorizing drugs and devices based on cost, type or method of administration.

  • 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.

  • 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.

  • Chinese Medicine Practitioner means a Chinese medicine practitioner who is duly registered with the Chinese Medicine Council of Hong Kong pursuant to the Chinese Medicine Ordinance (Cap. 549) of the laws of Hong Kong, but excluding the Insured Person, the Policyholder, an insurance intermediary, an employer, employee, Immediate Family Member or business partner of the Policyholder and/or Insured Person.

  • Agricultural product means the products listed in Annex I to the Treaty, except fishery and aquaculture products listed in Annex I to Regulation (EU) No 1379/2013 of the European Parliament and of the Council of 11 December 2013;

  • Physical therapy licensing board or "licensing board" means the agency of a state that is responsible for the licensing and regulation of physical therapists and physical therapist assistants.

  • EUMA means the “SAP Delivered Support Agreement” which sets out the terms and conditions under which SAP provides support to End Users and which will be provided by SAP on a deal by deal basis.

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

  • international application means an application filed under this Treaty;

  • agricultural products means an animal or plant or a product, including any food or drink that is wholly or partly derived from an animal or plant, and includes all after acquired Agricultural Products of the Producer, or any proceeds therefore.

  • 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:

  • Union territory means the territory of—

  • Medical marijuana waste or "waste" means unused,

  • Commercial solid waste means all types of solid waste generated by stores, offices, restaurants, warehouses, and other nonmanufacturing activities, excluding residential and industrial wastes.

  • Radiologic technologist, limited means an individual, other than a licensed radiologic technologist,