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รับรองรายงาน อย. 10 Feb 2015
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Utai Sukviwatsirikul
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พรเอนก ตาดทอง, โรคและอันตรายของการดำน้ำและการรักษา Hyperbaric Oxygen Therapy,
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The International Pharmaceutical Federation (FIP) first adopted the guidelines for Good Pharmaceutical Practice in 1993. These guidelines were developed as a reference to be used by national pharmaceutical organisations, governments, and international pharmaceutical organizations to set up nationally accepted standards of Good Pharmacy Practice. A revised version of this document was endorsed by WHO in 1997 and subsequently approved by the FIP Council in 1997. In 2011, FIP and WHO adopted an updated version of Good Pharmacy Practice entitled "Joint FIP/WHO guidelines on good pharmacy practice: standards for quality of pharmacy services". Full reference: Joint FIP/WHO guidelines on good pharmacy practice: standards for quality of pharmacy services. WHO Technical Report Series, No. 961, 2011. Geneva: World Health Organization, 2011. In this document, the aim of pharmacy practice aim is defined as to "contribute to health improvement and to help patients with health problems to make the best use of their medicines." GPP is defined as "the practice of pharmacy that responds to the needs of the people who use the pharmacists’ services to provide optimal, evidence-based care. To support this practice it is essential that there be an established national framework of quality standards and guidelines." The 2011 GPP document underlines the requirements of Good Pharmacy Practice and how to set standards required for GPP, (which also imply a quality management framework and a strategic plan for developing services). GPP are organised around 4 major roles for pharmacists Role 1: Prepare, obtain, store, secure, distribute, administer, dispense and dispose of medical products Role 2: Provide effective medication therapy management Role 3: Maintain and improve professional performance Role 4: Contribute to improve effectiveness of the health-care system and public health Each function is structured in several roles, and for each role, a list of minimum national standards to be established have been set. WHO/FIP GPP should serve as a guidance document for the development of specific standards of GPP at national levels by national pharmacists associations and other related stakeholders. When establishing minimum standards on GPP, it is important to define the roles played by pharmacists, as expected by patients and society. Secondly, relevant functions for which pharmacists have direct responsibility and accountability need to be determined within each role. Thirdly, minimum national standards should then be established, based upon the need to demonstrate competency in a set of activities supporting each function and role. Source of info: http://www.fip.org/good_pharmacy_practice
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The International Pharmaceutical Federation (FIP) first adopted the guidelines for Good Pharmaceutical Practice in 1993. These guidelines were developed as a reference to be used by national pharmaceutical organisations, governments, and international pharmaceutical organizations to set up nationally accepted standards of Good Pharmacy Practice. A revised version of this document was endorsed by WHO in 1997 and subsequently approved by the FIP Council in 1997. In 2011, FIP and WHO adopted an updated version of Good Pharmacy Practice entitled "Joint FIP/WHO guidelines on good pharmacy practice: standards for quality of pharmacy services". Full reference: Joint FIP/WHO guidelines on good pharmacy practice: standards for quality of pharmacy services. WHO Technical Report Series, No. 961, 2011. Geneva: World Health Organization, 2011. In this document, the aim of pharmacy practice aim is defined as to "contribute to health improvement and to help patients with health problems to make the best use of their medicines." GPP is defined as "the practice of pharmacy that responds to the needs of the people who use the pharmacists’ services to provide optimal, evidence-based care. To support this practice it is essential that there be an established national framework of quality standards and guidelines." The 2011 GPP document underlines the requirements of Good Pharmacy Practice and how to set standards required for GPP, (which also imply a quality management framework and a strategic plan for developing services). GPP are organised around 4 major roles for pharmacists Role 1: Prepare, obtain, store, secure, distribute, administer, dispense and dispose of medical products Role 2: Provide effective medication therapy management Role 3: Maintain and improve professional performance Role 4: Contribute to improve effectiveness of the health-care system and public health Each function is structured in several roles, and for each role, a list of minimum national standards to be established have been set. WHO/FIP GPP should serve as a guidance document for the development of specific standards of GPP at national levels by national pharmacists associations and other related stakeholders. When establishing minimum standards on GPP, it is important to define the roles played by pharmacists, as expected by patients and society. Secondly, relevant functions for which pharmacists have direct responsibility and accountability need to be determined within each role. Thirdly, minimum national standards should then be established, based upon the need to demonstrate competency in a set of activities supporting each function and role. Source of info: http://www.fip.org/good_pharmacy_practice
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Saccharomyces boulardii in the prevention of antibiotic-associated diarrhoea in children: a randomized double-blind placebo-controlled trial M. KOTOWSKA, P. ALBRECHT & H. SZAJEWSKA Department of Pediatric Gastroenterology and Nutrition, The Medical University of Warsaw, Warsaw, Poland Accepted for publication 24 November 2004
Saccharomyces boulardii in the prevention of antibiotic-associated diarrhoea ...
Saccharomyces boulardii in the prevention of antibiotic-associated diarrhoea ...
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