Pharmacy and Drug Act definition

Pharmacy and Drug Act means the Pharmacy and Drug Act, R.S.A. 2000, c. P- 13;
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Pharmacy and Drug Act means the Pharmacy and Xxxx Xxx, XXX 0000, c P- 13;
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Examples of Pharmacy and Drug Act in a sentence

  • The dispensary of a satellite pharmacy must meet the size and equipment requirements of a dispensary in a community pharmacy as outlined in the regulations to the Pharmacy and Drug Act and these standards.

  • This does not include the investments in the plantations themselves or infrastructures.

  • A licensee must ensure that drugs are kept in the appropriate locations within the prescription department, having regard for their scheduling under Part 4 of the Pharmacy and Drug Act.

  • KFC Industries Private Limited permits it to undertake similar business to our business, which may create a potential conflict of interest and which in turn, may have an implication on our operations and profits.

  • The Hearing Tribunal finds that the allegation set out in the Notice of Hearing is proven, and that the conduct constitutes unprofessional conduct as defined in the HPA and in the Pharmacy and Drug Act.

  • Their services are legalized by various instruments that include: The Medical and Dental Practitioners Statute (1996), the Nurses and Midwives Statute (1996), the Pharmacy and Drug Act (1970) and the Allied Health Professionals Statute (1996), which provide for licensing and other regulatory support.

  • Section 150(1) to (3) and Schedule 19 proclaimed in force on the coming into force of the Pharmacy and Drug Act.

  • According to the Pharmacy and Drug Act and its regulation, this includes, but is not limited to• a change in the licensee or proprietor, • a pharmacy renovation or relocation, • a change in the types of pharmacy services provided, • a change in the employment of any regulated pharmacy professional at the pharmacy, • a change in the hours of operation, and • a request to store patient records at a location other than the pharmacy.

  • Mr. Jardine argued that record keeping is a fundamental act of dispensing and the standards emphasize that.• Sections 1(1)(p)(i), 1(1)(p)(ii), 1(1)(p)(ix), 10(1)(a), 10(1)(d)(iv) and 10(1.1) of the Pharmacy and Drug Act;Mr. Jardine argued that allegations against a licensee are allegations of misconduct under the Pharmacy and Drug Act.

  • Despite article 4.1(a), this Agreement is not automatically terminated if: a community pharmacy licence has been issued by the College to a new licensee for the Community Pharmacy and the new licensee has affirmed this Agreement in writing; or the Community Pharmacy is, with the permission of the Registrar, being operated under the personal management, control and direction of another pharmacist under section 14(2) of the Pharmacy and Drug Act and that pharmacist has affirmed this Agreement in writing.

Related to Pharmacy and Drug Act

  • New Drug Application means a New Drug Application filed with the FDA in accordance with Applicable Law.

  • 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).

  • Drug abuse means any pattern of pathological use of drugs that causes impairment in social or occupational functioning, or that produces physiological dependency evidenced by physical tolerance or by physical symptoms when it is withdrawn.

  • FD&C Act means the U.S. Federal Food, Drug and Cosmetic Act, as amended, and the regulations promulgated thereunder.

  • MHLW means the Ministry of Health, Labour and Welfare of Japan, or the successor thereto.

  • Criminal drug statute means a Federal or non-Federal criminal statute involving the manufacture, distribution, dispensing, possession or use of any controlled substance.

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

  • Drug Application means a new drug application, an abbreviated drug application, or a product license application for any Product, as appropriate, as those terms are defined in the FDCA.

  • FDA means the United States Food and Drug Administration.

  • Biologics License Application or “BLA” means an application requesting permission from the FDA to introduce, or deliver for introduction, a biological product into interstate commerce, or any similar application or submission for marketing authorization of a product filed with a Regulatory Authority to obtain Regulatory Approval for such product in a country or group of countries.

  • HITECH Act means the Health Information Technology for Economic and Clinical Health Act, TitleXIII, Subtitle D, Part 1 & 2 of the American Recovery and Reinvestment Act of 2009.

  • national regulatory authority means the body or bodies charged by a Member State with any of the regulatory tasks assigned in this Directive and the Specific Directives;

  • Legend drug or "prescription drug" means any drug or device that has been determined to be unsafe for self- medication or any drug or device that bears or is required to bear the legend:

  • FDA Act means the U.S. Federal Food, Drug and Cosmetic Act, as amended, and the rules and regulations promulgated thereunder.

  • 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.

  • Prescription drug order means a lawful order of a practitioner for a drug or device for a specific patient that is communicated to a pharmacist.

  • Drug addiction means a disease characterized by a

  • Legend drugs means any drugs which are required by state

  • Occupational Health and Safety Act means the Occupational Health and Safety Act, 1993 (Act No 85 of 1993);

  • National Ambient Air Quality Standards or “NAAQS” means national ambient air quality standards that are promulgated pursuant to Section 109 of the Act, 42 U.S.C. § 7409.

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

  • FMC Act means the Financial Markets Conduct Act 2013.

  • Federal Aviation Act means the sections of Title 49 of the United States Code relating to aviation, as amended and in effect from time to time, or any similar legislation of the United States of America enacted in substitution or replacement thereof.

  • 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.

  • Act of 1997 means the Taxes Consolidation Act 1997;

  • Rail Safety Act means the Rail Safety Act 1998 (WA);