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Author: British Pharmacopoeia Commission
Publisher:
Published: 2003
Total Pages: 960
ISBN-13: 9780113225958
DOWNLOAD EBOOKThis three volume collection with CD-ROM contains the authoritative standard reference for medicines in the United Kingdom. It provides information on the quality of substances used throughout medicine and pharmaceutics. Two volumes contain the Pharmacopoeia while a third volume presents British Pharmacopoeia (Veterinary).
Author: Anthony C. Cartwright
Publisher: Routledge
Published: 2016-03-09
Total Pages: 281
ISBN-13: 1317039785
DOWNLOAD EBOOKThe British Pharmacopoeia has provided official standards for the quality of substances, medicinal products and articles used in medicine since its first publication in 1864. It is used in over 100 countries and remains an essential global reference in pharmaceutical research and development and quality control. This book explores how these standards have been achieved through a comprehensive review of the history and development of the pharmacopoeias in the UK, from the early London, Edinburgh and Dublin national pharmacopoeias to the creation of the British Pharmacopoeia and its evolution over 150 years. Trade in medicinal substances and products has always been global, and the British Pharmacopoeia is placed in its global context as an instrument of the British Empire as it first sought to cover the needs of countries such as India and latterly as part of its role in international harmonisation of standards in Europe and elsewhere. The changing contents of the pharmacopoeias over this period reflect the changes in medical practice and the development of dosage forms from products dispensed by pharmacists to commercially manufactured products, from tinctures to the latest monoclonal antibody products. The book will be of equal value to historians of medicine and pharmacy as to practitioners of medicine, pharmacy and pharmaceutical analytical chemistry.
Author: Great Britain. Medicines Commission
Publisher: Bernan Press(PA)
Published: 1996
Total Pages: 284
ISBN-13:
DOWNLOAD EBOOKAuthor: Gary Huckabay
Publisher: Potomac Books
Published: 2003-02
Total Pages: 564
ISBN-13: 9781574885613
DOWNLOAD EBOOKIn-depth statistics and predictions for every major league team and player.
Author:
Publisher:
Published: 2004
Total Pages: 326
ISBN-13:
DOWNLOAD EBOOKAuthor: British Pharmacopoeia Commission
Publisher:
Published: 2020-07-30
Total Pages:
ISBN-13: 9780113230846
DOWNLOAD EBOOKUpdated annually, the British Pharmacopoeia (BP) is the only comprehensive collection of authoritative official standards for UK pharmaceutical substances and medicinal products. It includes approximately 4,000 monographs which are legally enforced by the Human Medicines Regulations 2012. Where a BP monograph exists, medicinal products or active pharmaceutical ingredients sold or supplied in the UK must comply with the relevant monograph.All monographs and requirements of the European Pharmacopoeia (Ph. Eur.) are reproduced in the BP, making the BP a convenient and fully comprehensive set of standards that can be used across Europe and beyond.
Author: Sanjay Kumar Jain
Publisher: Elsevier Health Sciences
Published: 2011-08-23
Total Pages: 778
ISBN-13: 8131232662
DOWNLOAD EBOOKThis adaptation of Bentley's Textbook of Pharmaceutics follows the same goals as those of the previous edition, albeit in a new look. The content of the old edition has been updated and expanded and several new chapters, viz. Complexations, Stability Testing as per ICH Guidelines, Parenteral Formulations, New Drug Delivery Systems and Pilot Plant Manufacturing, have been included, with an intention to make the book more informative for the modern pharmacists. The book has six sections: - Section I deals with the physicochemical principles. Two new chapters: Complexations and ICH Guidelines for Stability Testing, have been added to make it more informative. - Section II conveys the information regarding pharmaceutical unit operations and processes. - Section III describes the area of pharmaceutical practice. Extensive recent updates have been included in many chapters of this section. Two new chapters: Parenteral Formulations and New Drug Delivery Systems, have been added. - Section IV contains radioactivity principles and applications. - Section V deals with microbiology and animal products. - Section VI contains the formulation and packaging aspects of pharmaceuticals. Pilot Plant Manufacturing concepts are added as a new chapter, which may be beneficial to readers to understand the art of designing of a plant from the pilot plant model.
Author: Institute of Medicine
Publisher: National Academies Press
Published: 2013-06-20
Total Pages: 377
ISBN-13: 0309269393
DOWNLOAD EBOOKThe adulteration and fraudulent manufacture of medicines is an old problem, vastly aggravated by modern manufacturing and trade. In the last decade, impotent antimicrobial drugs have compromised the treatment of many deadly diseases in poor countries. More recently, negligent production at a Massachusetts compounding pharmacy sickened hundreds of Americans. While the national drugs regulatory authority (hereafter, the regulatory authority) is responsible for the safety of a country's drug supply, no single country can entirely guarantee this today. The once common use of the term counterfeit to describe any drug that is not what it claims to be is at the heart of the argument. In a narrow, legal sense a counterfeit drug is one that infringes on a registered trademark. The lay meaning is much broader, including any drug made with intentional deceit. Some generic drug companies and civil society groups object to calling bad medicines counterfeit, seeing it as the deliberate conflation of public health and intellectual property concerns. Countering the Problem of Falsified and Substandard Drugs accepts the narrow meaning of counterfeit, and, because the nuances of trademark infringement must be dealt with by courts, case by case, the report does not discuss the problem of counterfeit medicines.
Author: https://www.chinesestandard.net
Publisher: https://www.chinesestandard.net
Published: 2015-04-18
Total Pages: 21
ISBN-13:
DOWNLOAD EBOOKThis standard specifies classification, requirements, analysis methods, inspection rules, and marking, packaging, transportation, and storage of citric acid for food processing. This standard is applicable to citric acid products made of starchy materials or sugar-containing materials, and such citric acid is mainly used as sour agent, anti-oxidation synergist and flavouring agent for food processing.
Author: British pharmacopoeia commission
Publisher:
Published: 1996
Total Pages: 284
ISBN-13: 9780113219933
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