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

  • 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.

  • To quote from the Accreditation Standards of the Pharmaceutical Society of Ireland (PSI), "The purpose of undergraduate pharmacy education (the pharmacy degree programme) is to produce pharmacy graduates who have the knowledge, skills and attributes to safely participate in the National Pharmacy Internship Programme (NPIP).

  • The National Pharmacy Internship Programme and the Professional Registration Examination are the responsibility of the Pharmaceutical Society of Ireland.

  • Please list any Health or Social Care Profession regulatory bodies you have been registered with within the last 5 years (General Pharmceutical Council, Pharmaceutical Society of Ireland etc).

  • Pharmaceutical Society of Ireland Core Competency Framework for Pharmacists [Online] Available from: http://www.thepsi.ie/Libraries/Publications [Accessed 22 Apr.

  • Be a registered Pharmacist with the Pharmaceutical Society of Ireland (PSI) or be entitled to be so registeredAnd Have at least three years satisfactory post registration hospital experience And Possess the requisite knowledge and ability (including a high standard of suitability and management ability) for the proper discharge of the duties of the office.

  • The Pharmaceutical Society of Ireland require, as part of the Interim Accreditation Standards for the Level 8 Bachelor Degree (2012), that success in a formal examination of pharmacy law and a summative assessment of ethics and professionalism in the final year shall be a condition for the award of the degree.

  • Module 3: Learning in the workplace.Module 4: Managing the intern over time.The Council of the Pharmaceutical Society of Ireland requires all prospective tutors to complete a tutor training programme prior to registration as a tutor.

  • The Pharmacy Practice Guidance Manual – a self-audit tool for pharmacists and pharmacy owners issued by the Pharmaceutical Society of Ireland Standards and Practice Unit is a useful guide for this activity.

  • In the event FHWA or any other Federal agency is named in litigation related to matters under this MOU or the United States intervenes in the litigation, ODOT agrees to coordinate with DOJ in the defense of that action.

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 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” shall mean one or more of the following active pharmaceutical ingredients: tenofovir alafenamide (“TAF”), tenofovir disoproxil fumarate (“TDF”), elvitegravir (“EVG”), and cobicistat (“COBI”).

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

  • 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.

  • Clinical means having a significant relationship, whether real or potential, direct or indirect, to the actual rendering or outcome of dental care, the practice of dentistry, or the quality of dental care being rendered to a patient;

  • 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.

  • Clinical Development means the conduct of clinical trials in humans to assess the dosing, safety and/or efficacy of the Product, including but not limited to Phase I Clinical Trials, Phase II Clinical Trials, Phase Ill Clinical Trials and Phase IV Clinical Trials.

  • 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:

  • Competent Supervisory Authority means a supervisory authority which has jurisdiction in relation to the activities of a controller or processor under European data protection law in a particular Member State;

  • Research and development facility means an establishment engaged in laboratory, scientific, or experimental testing and development related to new products, new uses for existing products, or improving existing products. The term does not include an establishment engaged in efficiency surveys, management studies, consumer surveys, economic surveys, advertising, promotion, banking, or research in connection with literary, historical, or similar projects.

  • 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,

  • Public Procurement Regulatory Authority (PPRA) means the Government Agency responsible for oversight of public procurement.