Pharmacy and Drug Regulation definition

Pharmacy and Drug Regulation means the Pharmacy and Drug Regulation, AR 240/2006;
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Examples of Pharmacy and Drug Regulation in a sentence

  • This Agreement is designed to address the regulatory requirements under section 19(a) of the Pharmacy and Drug Regulation and is not designed to address the commercial relationship between the parties, which may be governed by a commercial agreement that is not inconsistent with this Agreement; and available to the Registrar to ensure compliance with clause (a).

  • It also provides a graph of the students’ self-assessment as wellas a consolidated score from the other individuals.

  • To ensure that this Agreement remains consistent with any new directions of the Council of the College made under section 19(a)(i) of the Pharmacy and Drug Regulation after the effective date of this Agreement, the parties agree to renegotiate the terms of this Agreement to comply with those new directions and to make the necessary amendments to this Agreement in accordance with articles 5.4 and 18.3 within 30 working days of the issuance of any new directions.

  • The requirement for compounding and repackaging agreements comes from Section 19 of the Pharmacy and Drug Regulation.

  • The cone of this quasi-isomorphism α is the four-term complex.1(−2) → Bs(−1) → Bs(1) → 1(2)Σ.We now prove that the notions of left and right λ-equivalence agree, so after this section we will simply write λ-equivalence.∈ →Lemma 7.4. Let BT,U SBimn be in cell λ, and let α : Σλ(1) FTn be a chain map.

  • 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).

  • In addition to any requirements under section 27(1) of the Pharmacy and Drug Regulation, if the Compounding and Repackaging Pharmacy’s licence is suspended, cancelled or otherwise termination, the Compounding and Repackaging Pharmacy must make arrangements to enable the Community Pharmacy to continue to access any records relating to the provision of the Services under this Agreement in accordance with the record keeping requirements of the College.

  • Helke; Tom Pfeilling team and he has lettered three »ergeant in the summer of 1940.ed away to win 72-45.

  • Transportation Security Administration (TSA) Pipeline Cybersecurity Standards• TSA Security Directive 2c; Section I: TSA has significantly revised the Security Directive initially issued in July 2021 to provide owner/operators with more flexibility to meet the intended security outcomes while ensuring sustainment of the cybersecurity enhancements accomplished through this Security Directive series.

  • An updated agreement will be required if there is a change to the Distributor classification or a Global Intermediary Identification Number (GIIN).

Related to Pharmacy and Drug Regulation

  • 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.

  • 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).

  • EU Regulation means a regulation within the meaning of Article 288 of the Treaty on the Functioning of the European Union;

  • 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;

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

  • 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.

  • FDA means the United States Food and Drug Administration.

  • 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.

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

  • 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.

  • PDMA means the Prescription Drug Marketing Act of 1987, as amended from time to time, together with any rules or regulations promulgated thereunder.

  • 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.

  • Council Regulation means Council Regulation (EC) No. 2100/94 of 27th July 1994 on Community plant variety rights;

  • Data Protection Regulation means Regulation (EU) 2016/679 of the European Parliament and of the Council of 27 April 20161 on the protection of natural persons with regard to the processing of personal data and on the free movement of such data, and repealing Directive 95/46/EC (General Data Protection Regulation);

  • Market Abuse Regulation means Regulation (EC) No …/… of the European Parliament and of the Council on insider dealing and market manipulation (market abuse);

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

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

  • 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.

  • SEBI Regulations means the Securities and Exchange Board of India (Listing Obligations and Disclosure Requirements) Regulations, 2015 together with the circulars issued thereunder, including any statutory modification(s) or re-enactment(s) thereof for the time being in force.

  • Automated drug dispensing system means a mechanical or electronic system that performs

  • Insurance Regulatory Authority means, with respect to any Insurance Subsidiary, the insurance department or similar Governmental Authority charged with regulating insurance companies or insurance holding companies, in its jurisdiction of domicile and, to the extent that it has regulatory authority over such Insurance Subsidiary, in each other jurisdiction in which such Insurance Subsidiary conducts business or is licensed to conduct business.

  • the Council Regulation means Council Regulation (EC) No.1083/2006 laying down general provisions on the European Regional Development Fund, the European Social Fund and the Cohesion Fund and repealing Regulation (EC) No.1260/1999(5);

  • MFDA means the Mutual Fund Dealers Association of Canada;

  • OHS Regulation means the Workers Compensation Act (British Columbia), including without limitation, the Occupational Health & Safety Regulation (BC Regulation 296/97, as amended by BC Regulation 185/99) enacted pursuant to such Act, all as such Act or Regulations are amended or re-enacted from time to time.

  • 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:

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