Good Pharmacy Practice definition

Good Pharmacy Practice means the rules of good pharmacy practice made from time to time by the South African Pharmacy Council in terms of section 35A(b)(ii) of the Pharmacy Act;
Sample 1Sample 2Sample 3
Good Pharmacy Practice means a set of principles and standards for practice at drug retailers (or pharmacies) with the aims of ensuring and improve the direct supply and retailing of safe and effective drugs to patients.
Sample 1
Good Pharmacy Practice means good Pharmacy
Sample 1

Examples of Good Pharmacy Practice in a sentence

  • National Good Pharmacy Practice Guidelines are not published by the government.

  • The Institution will authorize an employee and member of the Staff appropriately qualified to act as the pharmacist to secure proper handling and subsequent distribution of the Product as requested by the Investigator, and in accordance with Good Pharmacy Practice (Regulation No. 84/2008 Coll.), Applicable Laws and Regulations and the provisions of the Protocol.

  • Such a storage area must fall under the authority of the responsible pharmacist of the pharmacy of which it forms a part, and be operated in compliance with Good Pharmacy Practice.

  • Institution and Principal Investigator will ensure proper receipt, handling and storage, and dispensing of the Study Product and any other compounds by a duly qualified pharmacist according to Good Pharmacy Practice.

  • Talmud)• ePharmaciae (www.pharmaciae.org.za)• Essential Drug List and Standard Treatment Guidelines – PHC, Hospital and Paediatric (electronic copies provided)• Good Pharmacy Practice (GPP) (electronic copy available)• Guidelines for Good Wholesaling and Distribution Practices• Handbook on Injectable Drugs (L.Trissel)• Martindale: The Extra Pharmacopoeia (electronic copy provided)• Merck Manual or equivalent• MIMS / MDR• Pharmaceutical Calculations (H.

  • National Good Pharmacy Practice Guidelines are published by the government.

  • PL03: Premises Information Completed in FullYNN/AThe name of the pharmacy premises indicated The square meters of the pharmacy premises indicated The Good Pharmacy Practice checklist for the premises is completed in full The PL03 is signed iv.

  • As explained above, there are three institutions in Korea that are officially involved in performing energy demand forecast in cooperation with MOCIE.

  • Importance and awareness of the Good Pharmacy Practice from drugstore clients’ perspectives.

  • Self-assessment document based on Good Pharmacy Practice (GPP) assessment guidelines.


More Definitions of Good Pharmacy Practice

Good Pharmacy Practice means good Pharmacy practice guidelines issued by the Authority;
Sample 1Sample 2

Related to Good Pharmacy Practice

  • Collaborative pharmacy practice means a practice of pharmacy whereby one or more pharmacists have jointly agreed, on a voluntary basis, to work in conjunction with one or more practitioners under protocol whereby the pharmacist may perform certain pharmaceutical care functions authorized by the practitioner or practitioners under certain specified conditions or limitations.

  • Good Industry Practice means standards, practices, methods and procedures conforming to the Law and the exercise of the degree of skill and care, diligence, prudence and foresight which would reasonably and ordinarily be expected from a skilled and experienced person or body engaged within the relevant industry or business sector;

  • Good Manufacturing Practices means current good manufacturing practices, as set forth in 21 C.F.R. Parts 210 and 211.

  • Good Clinical Practices means the FDA’s standards for the design, conduct, performance, monitoring, auditing, recording, analysis, and reporting of clinical trials contained in 21 C.F.R. Part 50, 54, 56, 312, 314, 320, 812, and 814 and (ii) “Good Laboratory Practices” means the FDA’s standards for conducting non-clinical laboratory studies contained in 21 C.F.R. Part 58.

  • Good Laboratory Practices or “GLP” means the then-current Good Laboratory Practice (or similar standards) for the performance of laboratory activities for pharmaceutical products as are required by applicable Regulatory Authorities or Applicable Law. In the United States, Good Laboratory Practices are established through FDA regulations (including 21 C.F.R. Part 58), FDA guidance, FDA current review and inspection standards and current industry standards.

  • Good Industry Practices means the practices that would be adopted by, and the exercise of that degree of care, skill, diligence, prudence and foresight that reasonably would be expected from, a competent contractor in the international oil and gas industry experienced in performing work similar in nature, size, scope and complexity to the Work and under conditions comparable to those applicable to the Work, where such work is subject to, and such contractor is seeking to comply with, the standards and codes specified in the Contract or (to the extent that they are not so specified) such national or international standards and codes as are most applicable in the circumstances, and the applicable Law.

  • Proper practices means those set out in The Practitioners’ Guide

  • Current Good Manufacturing Practices or “cGMP” means applicable Good Manufacturing Practices as specified in the United States Code of Federal Regulations and/or the EU Good Manufacturing Guidelines, and any successor legislation from time to time, prevailing at the time of the manufacture of the Product.

  • Good Clinical Practice or “GCP” means the then current standards for clinical trials for pharmaceuticals, as set forth in the ICH guidelines and applicable regulations promulgated thereunder, as amended from time to time, and such standards of good clinical practice as are required by the European Union and other organizations and governmental agencies in countries in which a Licensed Product is intended to be sold to the extent such standards are not less stringent than the ICH guidelines.

  • Collaborative pharmacy practice agreement means a written and signed

  • Good Manufacturing Practice or “GMP” means the current good manufacturing practices applicable from time to time to the manufacturing of a Product or any intermediate thereof pursuant to Applicable Law.

  • Unfair labor practice means the commission of an act designated an unfair labor practice

  • Unsafe or unsound practice means a practice or conduct by a person licensed to engage in money transmission or an authorized delegate of such a person, which creates the likelihood of material loss, insolvency, or dissipation of the licensee’s assets, or otherwise materially prejudices the interests of its customers.

  • cGMP means current Good Manufacturing Practices as specified in the United States Code of Federal Regulations, ICH Guideline Q7A, or equivalent laws, rules, or regulations of an applicable Regulatory Authority at the time of manufacture.

  • Active practice means post-licensure practice at the level of licensure for which an applicant is seeking licensure in Virginia and shall include at least 360 hours of practice in a 12-month period.

  • Code of Good Practice means the generic codes or the sector codes as the case may be;

  • Prudent Industry Practices means, at a particular time, any of the practices, methods, standards of care, skill, safety and diligence, as the same may change from time to time, but applied in light of the facts known at the time, that are consistent with the general standards applied or utilized under comparable circumstances by a reasonably prudent operator, in a good and workmanlike manner, with due diligence and dispatch, in accordance with good midstream industry practice.

  • Community practice protocol means a written, executed agreement entered into voluntarily between an authorized pharmacist and a physician establishing drug therapy management for one or more of the pharmacist’s and physician’s patients residing in a community setting. A community practice protocol shall comply with the requirements of subrule 8.34(2).

  • Best Industry Practice means that degree of skill, care and foresight and operating practice that would reasonably and ordinarily be expected of a skilled and competent supplier of services engaged in the same type of undertaking as that of the Recipient or any contractors (as applicable) under the same or similar circumstances as those contemplated by this Agreement.

  • Best Practice means solutions, techniques, methods and approaches which are appropriate, cost-effective and state of the art (at Member State and sector level), and which are implemented at an operational scale and under conditions that allow the achievement of the impacts set out in the award criterion ’Impact’ first paragraph (see below).

  • Prudent Industry Practice means such practices, methods, acts, techniques, and standards as are in effect at the time in question that are consistent with (a) the standards generally followed by the United States pipeline and terminalling industries or (b) such higher standards as may be applied or followed by the Xxxxx Entities in the performance of similar tasks or projects, or by the Partnership Entities in the performance of similar tasks or projects.