Pharmacy and Drug Act definition

Pharmacy and Drug Act means the Pharmacy and Drug Act, R.S.A. 2000, c. P- 13;
Sample 1Sample 2Sample 3
Pharmacy and Drug Act means the Pharmacy and Xxxx Xxx, XXX 0000, c P- 13;
Sample 1Sample 2Sample 3

Examples of Pharmacy and Drug Act in a sentence

  • Despite article 4.1(a), this Agreement is not automatically terminated if the Institution Pharmacy is reinstated as an “institution pharmacy” as defined in the Pharmacy and Drug Act and the pharmacist in charge affirms this Agreement in writing and the parties have made all necessary amendments to this Agreement to reflect the granting of a community pharmacy licence to the Institution Pharmacy and the role of the licensee of the Institution Pharmacy.

  • These requirements correspond to sections of the• Pharmacy and Drug Act (PDA), • Pharmacy and Drug Regulation (PDR), • Standards for the Operation of Licensed Pharmacies (SOLP), and • Standards of Practice for Pharmacists and Pharmacy Technicians (SPPPT).

  • I, , of (name of applicant) (name of city/ town) in the Province of, an applicant for a pharmacy licence under(province) the Pharmacy and Drug Act, do solemnly declare:that I have not been convicted of an indictable offence related to misconduct, fraud or commercial matters within Canada or a similar offence outside Canada.

  • 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.

  • Lev Vegotsky is one example; his contribution to the emergence of autonomy lies in the notion of self- directed inner speech.”(p.

  • Those include Pharmacy and Drug Act 2001, related guidelines and the drug policy.

  • Pharmacy practice consultants (PPCs) role and authority arises from the Health Professions Act (HPA)and the Pharmacy and Drug Act (PDA).

  • Mr. Ibrahim’s conduct also breached Standard 1 of the Standards for the Operation of Licensed Pharmacies that also states the licensee must operate the pharmacy within the confines of the HPA, the Pharmacy and Drug Act and the Code of Ethics.

  • Mail order pharmacy and mail order pharmacy service are now defined in the Pharmacy and Drug Act: 1(1)(n.1) A “mail order pharmacy” means a community pharmacy with respect to which a mail order pharmacy license has been issued;1(1)(n.2) A “mail order pharmacy service” means a pharmacy service provided to or for a patient for which neither the patient nor the patient’s agent attends at the community pharmacy to receive the service.

  • These changes are limited to setting technical, operational, or administrative requirements and guidelines.We are also making changes to the Pharmacy and Drug Act to give the Alberta College of Pharmacy the flexibility in its oversight of pharmacies which will allow for a more pointed response to changes in the health care environment such as natural disasters, pandemics, or drug shortages.

Related to Pharmacy and Drug Act

  • New Drug Application means a new drug application in the United States for authorization to market a product, as defined in the applicable laws and regulations and submitted to the FDA.

  • 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 United States Federal Food, Drug and Cosmetic Act, as amended.

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

  • 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.

  • 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.

  • 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 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;

  • 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 subtitle VII of Title 49 of the United States Code, or any successor provision.

  • 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);

  • Drug Approval Application means an application for Regulatory Approval required before commercial sale of a Product as a pharmaceutical product in a regulatory jurisdiction.