Provincial Drug Programs definition

Provincial Drug Programs means Manitoba Pharmacare, Palliative Care Drug Access Program, Personal Care Home Drug Program, Family Services Drug Program, and Deductible Instalment Payment Program for Pharmacare (DIPPP) and any other program that the Minister may designate in the future to form part of the Provincial Drug Programs;
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Examples of Provincial Drug Programs in a sentence

  • CHANGES TO APPROVAL PROCESS AND EXPIRY DATES - EFFECTIVE OCTOBER 2017Effective October 1, 2017 many Part 3 drugs will no longer require EDS renewal for coverage underManitoba's Provincial Drug Programs (PDP) and the Employment and Income Assistance Drug Program (EIA).

  • Major health and social services expenditures are allocated to: Hospital Services, 31 percent; Social Services, 21 percent; Long Term Care, 10 percent; Physician Services, 12 percent; and other services such as Provincial Drug Programs, Public Health Nursing and Addiction Services, 26 percent.

  • Provincial Drug Programs has identified a situation of specific patient need, has preapproved an extemporaneous product (compound) recipe and assigned a Product Identification Number (PIN) to that extemporaneous product.

  • Letter from Patricia Caetano, Executive Director, Provincial Drug Programs, Manitoba Health, Seniors and Active Living, dated April 17, 2018.

  • The local system must support submitting multiple invoices to separate Provincial Drug Programs as part of a single invoice to account for cases where a Patient has multiple applicable coverages.

  • I/WE consent to Manitoba Health -- including the Deductible Instalment Payment Program for Pharmacare and Provincial Drug Programs -- and Manitoba Hydro collecting from and disclosing to each other personal information, personal health information, financial and other information about me/us that is necessary to deal with my/our application to be enrolled in the payment program and to administer and enforce the payment program.

  • Generic drug submission requirements ensures generic drug pricing in Manitoba is equitable with other Canadian jurisdictions. Provincial Drug Programs representatives participated on advisory committees to the Canadian Agency for Drugs and Technologies in Health (CADTH) Common Drug Review and pan-Canadian Oncology Drug Review.

  • Generic drug submission requirements ensures generic drug pricing in Manitoba is equitable with other Canadian jurisdictions. Provincial Drug Programs representatives participated on advisory committees to the Canadian Agency for Drugs and Technologies in Health, and advisory committees to the pan-Canadian Oncology Drug Review.

  • This type of estimation is less reliable as it often leads to more than 10 fold variation in the quantity estimated6.

Related to Provincial Drug Programs

  • Provincial Minister means the member of the Cabinet of the Province of Western Cape responsible for local government;

  • provincial department ’ means a department listed in Schedule 2 of the Public Service Act, 1994 (Proclamation No. 103 of 1994), which falls within a provincial administration listed in Schedule 1 to that Act; 10

  • FFDCA means the United States Federal Food, Drug, and Cosmetic Act, 21 U.S.C. §301 et seq., as amended from time to time, together with any rules, regulations and requirements promulgated thereunder (including all additions, supplements, extensions, and modifications thereto).

  • Loss Absorption Regulations means, at any time, the laws, regulations, requirements, guidelines, rules, standards and policies relating to minimum requirements for own funds and eligible liabilities and/or loss absorbing capacity instruments of the Kingdom of Belgium, the Relevant Regulator, the Resolution Authority, the Financial Stability Board and/or of the European Parliament or of the Council of the European Union then in effect in the Kingdom of Belgium including, without limitation to the generality of the foregoing, any delegated or implementing acts (such as regulatory technical standards) adopted by the European Commission and any regulations, requirements, guidelines, rules, standards and policies relating to minimum requirements for own funds and eligible liabilities and/or loss absorbing capacity instruments adopted by the Relevant Regulator and/or the Resolution Authority from time to time (whether or not such regulations, requirements, guidelines, rules, standards or policies are applied generally or specifically to the Issuer or to the Group).

  • Provincial Council means a council established for a non-metropolitan province in terms of section 269 of the Constitution;

  • Provincial Government means the Government of a Province of Pakistan;

  • Government Apprenticeship Programme “ means training which is funded by the Government via the National Apprenticeship Service.

  • Health Canada means the department of the Canadian Government known as Health Canada and includes, among other relevant branches, the Therapeutic Products Directorate and the Health Products and Food Branch Inspectorate;

  • FDA means the United States Food and Drug Administration and any successor agency thereto.

  • provincial legislation means legislation contemplated in section 10 of the Act promulgated by the Province;

  • Public health authority means an agency or authority of the United States, a state, a territory, a political subdivision of a state or territory, an Indian tribe, or a foreign government, or a person or entity acting under a grant of authority from or contract with such public agency, including the employees or agents of such public agency or its contractors or persons or entities to whom it has granted authority, that is responsible for public health matters as part of its official mandate.

  • Foreign Financial Regulatory Authority shall have the meaning given by Section 2(a)(50) of the 0000 Xxx.

  • EMA means the European Medicines Agency or any successor agency thereto.

  • Nuclear Regulatory Commission (NRC) means the U.S. Nuclear Regulatory Commission or its duly authorized representatives.

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

  • Relevant Electric Retail Regulatory Authority means an entity that has jurisdiction over and establishes prices and policies for competition for providers of retail electric service to end- customers, such as the city council for a municipal utility, the governing board of a cooperative utility, the state public utility commission or any other such entity.

  • MHLW means the Japanese Ministry of Health, Labour and Welfare, and any successor agency thereto.

  • Occupational Safety and Health Law means any Legal Requirement designed to provide safe and healthful working conditions and to reduce occupational safety and health hazards, and any program, whether governmental or private (including those promulgated or sponsored by industry associations and insurance companies), designed to provide safe and healthful working conditions.

  • Government Programs means (i) the Medicare and Medicaid Programs, (ii) the United States Department of Defense Civilian Health Program for Uniformed Services and (iii) other similar foreign or domestic Federal, state or local reimbursement or governmental health care programs.

  • Licensed health care practitioner means a physician, as defined in Section 1861(r)(1) of the Social Security Act, a registered professional nurse, licensed social worker or other individual who meets requirements prescribed by the Secretary of the Treasury.

  • PDMA means the Prescription Drug Marketing Act of 1987, as amended, and the regulations promulgated thereunder from time to time.

  • foreign regulatory authority means a securities commission, exchange or other securities market regulatory authority in a designated foreign jurisdiction;

  • Food and food ingredients means substances, whether in liquid, concentrated, solid, frozen, dried, or dehydrated form, that are sold for ingestion or chewing by humans and are consumed for their taste or nutritional value. Food and food ingredients do not include alcoholic beverages and tobacco.

  • Prescription drug order means an original or new order from a practitioner for drugs, drug-related devices or treatment for a human or animal, including orders issued through collaborative care agreements. Lawful prescriptions result from a valid practitioner-patient relationship, are intended to address a legitimate medical need, and fall within the prescribing practitioner's scope of professional practice;

  • Canadian Securities Regulatory Authorities means the securities regulatory authorities in each of the provinces and territories of Canada;

  • Council of governments means a decision-making body in each county composed of membership including the county governing body and the mayors of each municipality in the county.