Автор: Rostron, Chris (honorary Research Fellow In The School Of Pharmacy And Biomolecular Sciences At Liverpool John Moores University, Honorary Research Fe Название: Drug design & development paperback ISBN: 0198749317 ISBN-13(EAN): 9780198749318 Издательство: Oxford Academ Рейтинг: Цена: 6651.00 р. Наличие на складе: Есть у поставщика Поставка под заказ.
Описание: Drug Design and Development outlines the processes involved in the design and development of new drugs and emphasises the significance of these processes to the practice of pharmacy.
Автор: V.N. Raje Название: Pharmaceutics II For Second Year Diploma In Pharmacy ISBN: 9386478455 ISBN-13(EAN): 9789386478450 Издательство: CBS India Рейтинг: Цена: 2456.00 р. Наличие на складе: Нет в наличии.
Автор: V.N. Raje Название: Pharmacognosy for First Year Diploma in Pharmacy ISBN: 938647851X ISBN-13(EAN): 9789386478511 Издательство: CBS India Рейтинг: Цена: 2613.00 р. Наличие на складе: Нет в наличии.
Описание: Chapter 1 examines the actions of drug companies in raising prescription drug prices in the United States, as well as the effects of these actions on the Federal and state budgets, and on American families. Chapter 2 addresses frequently asked questions about government and private-sector policies that affect drug prices and availability. Among the prescription drug topics covered are federally funded research and development, regulation of direct-to-consumer advertising, legal restrictions on reimportation, and federal price negotiation. The 340B Drug Pricing Program requires drug manufacturers to sell outpatient drugs at discounted prices to covered entitiesaeligible clinics, hospitals, and othersain order to have their drugs covered by Medicaid. Covered entities are only allowed to provide 340B drugs to certain eligible patients. Chapter 3 reviews the Health Resources and Services Administrations (HRSA) oversight of the 340B Program to ensure compliance with program rules. In 2017, nearly 60% of U.S. adults aged 18a64 reported being prescribed medication in the past 12 months. Approximately 70% of prescription medications carry out-of-pocket costs. Strategies to reduce prescription drug costs at the individual level are discussed in chapters 4 and 5. Each year, Americans pay more for prescription drugs, and rising drug prices have a disproportionate impact on older Americans. Chapter 6 examines the history of rising drug prices for the brand-name drugs most commonly prescribed for seniors. Generic drugsacopies of brand-name drugsalead to significant cost savings. Before a generic drug can be marketed, FDA must approve the generic drug application. According to FDA, applications go through an average of three cycles of review before being approved, which may take years. Chapter 7 examines 1) the first review cycle approval rate of generic drug applications in recent years and factors that may have contributed to whether applications were approved; and 2) changes FDA has made to increase the first review cycle approval rate.
Автор: Anees Ahmad Siddiqui, Harish Kumar, Subuhi Khisal Название: Computer-Aided Drug Design ISBN: 9387964353 ISBN-13(EAN): 9789387964358 Издательство: CBS India Рейтинг: Цена: 12488.00 р. Наличие на складе: Нет в наличии.
Описание: This book is compiled to cover all the topics of computer-aided drug design for pharmacy professionals in industry. Written in easy to understand language, the text is well supplemented by illustrative diagrams, tables, molecular structures of drugs and their synthesis, providing a clear understanding of the subject to the reader.
Автор: Meharban Singh, Ashok K. Deorari Название: Drug Dosages in Children ISBN: 9388902661 ISBN-13(EAN): 9789388902663 Издательство: CBS India Рейтинг: Цена: 3658.00 р. Наличие на складе: Нет в наличии.
Описание: Serves as a ready-reckoner of drug dosages for young residents and practising pediatricians which will instil confidence in their prescribing abilities and reduce the incidence of avoidable side effects of drugs. It provides brief Information on the pharmacokinetics of drugs with an emphasis on the advantages and disadvantages of various routes of administration, drug absorption, distribution, bioavailabillty, tissue binding, half-life and metabolism and excretion. The drugs have been listed alphabetically with dally dosages per unit body weight, frequency, and route of administration. Important cautions, contraindications and adverse effects of selected drugs have been provided. Trade names of formulations from standard pharmaceutical companies along with their products and strengths are also given.
Название: Davis`s Drug Guide for Nurses ISBN: 171964005X ISBN-13(EAN): 9781719640053 Издательство: Marston Book Services Рейтинг: Цена: 9692.00 р. Наличие на складе: Поставка под заказ.
Описание: Ideal for courses in nursing programs covering drug and/or drug administration. Also serves practicing nurses Monographs provide user-friendly 'Cure' and 'Care' organization to allow users to find must-know information quickly and easily Designed to focus on patient safety by calling out 'High Alert' drugs and using red, capitalized letters for life-threatening side effects Includes 1-year free access to Davis's Drug Guide Online , powered by Unbound Medicine, a database of over 5,000 drugs and FDA news alerts Canadian-specific content, including Canadian trade Names and drugs specifically approved for use in Canada A wealth of online resources including an audio pronunciation library, calculators, and video clips illustrating the safe administration of medications
Автор: Papiya Bigonia Название: Drug Regulatory Affairs ISBN: 9388902963 ISBN-13(EAN): 9789388902960 Издательство: CBS India Рейтинг: Цена: 5173.00 р. Наличие на складе: Нет в наличии.
Описание: Drug Regulatory Affairs is a compilation of fundamental concepts pertaining to pharmaceutical drug regulation. Governments protect public health by strictly controlling the safety and efficacy of human medicine, veterinary medicines, medical devices, cosmetics and complementary medicines. Companies responsible for the discovery, testing, manufacture and marketing of these products must ensure sale of safe and effective products. Drug Regulatory Affairs refers to fulfilment of all aspects of drug regulations within the pharmaceutical companies from development process to finished product marketing.
The book provides a sound basis on understanding of international drug regulatory guidelines controlling the quality, safety and purity of marketed drugs. The content of this book covers the syllabus of pharmacy undergraduate and postgraduate course content of drug regulatory affairs. The text focuses on delivering updated and reviewed up-to-date information on current global regulatory guidelines. The book contains information that is substantial to a comprehensive understanding of regulatory affairs and the practice in pharmaceutical industry.
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