Контакты/Проезд  Доставка и Оплата Помощь/Возврат
История
  +7(495) 980-12-10
  пн-пт: 10-18 сб,вс: 11-18
  shop@logobook.ru
   
    Поиск книг                    Поиск по списку ISBN Расширенный поиск    
Найти
  Зарубежные издательства Российские издательства  
Авторы | Каталог книг | Издательства | Новинки | Учебная литература | Акции | Хиты | |
 

Topical Drug Bioavailability, Bioequivalence, and Penetration, Vinod P. Shah; Howard I. Maibach; John Jenner


Варианты приобретения
Цена: 22359.00р.
Кол-во:
Наличие: Поставка под заказ.  Есть в наличии на складе поставщика.
Склад Америка: Есть  
При оформлении заказа до: 2025-07-28
Ориентировочная дата поставки: Август-начало Сентября
При условии наличия книги у поставщика.

Добавить в корзину
в Мои желания

Автор: Vinod P. Shah; Howard I. Maibach; John Jenner
Название:  Topical Drug Bioavailability, Bioequivalence, and Penetration
ISBN: 9781493912889
Издательство: Springer
Классификация:




ISBN-10: 1493912887
Обложка/Формат: Hardcover
Страницы: 402
Вес: 0.78 кг.
Дата издания: 30.01.2015
Язык: English
Издание: 2nd ed. 2014
Иллюстрации: 72 tables, black and white; 16 illustrations, color; 48 illustrations, black and white; xiii, 402 p. 64 illus., 16 illus. in color.
Размер: 234 x 156 x 24
Читательская аудитория: Professional & vocational
Основная тема: Pharmacology/Toxicology
Ссылка на Издательство: Link
Рейтинг:
Поставляется из: Германии
Описание: This authoritative volume explores advances in the techniques used to measure percutaneous penetration of drugs and chemicals to assess bioavailability and bioequivalence and discusses how they have been used in clinical and scientific investigations. Seven comprehensive sections examine topics including in vitro drug release, topical drugs products, clinical studies, and guidelines and workshop reports, among others. The book also describes how targeted transdermal drug delivery and more sophisticated mathematical modelling can aid in understanding the bioavailability of transdermal drugs. The first edition of this book was an important reference guide for researchers working to define the effectiveness and safety of drugs and chemicals that penetrated the skin. This second edition contains cutting-edge advances in the field and is a key resource to those seeking to define the bioavailability and bioequivalence of percutaneously active compounds to improve scientific and clinical investigation and regulation.
Дополнительное описание: 1 Percutaneous Absorption.- 2 Animal Models for Percutaneous Absorption.- 3 Mitigating Dermal Exposure to Agrochemicals.- 4 Importance of In Vitro Drug Release.- 5 Diffusion Cell Design.- 6 In Vitro Product Quality Tests and Product Performance Tests for



Bioequivalence and Statistics in Clinical Pharmacology

Автор: Patterson
Название: Bioequivalence and Statistics in Clinical Pharmacology
ISBN: 1584885300 ISBN-13(EAN): 9781584885306
Издательство: Taylor&Francis
Рейтинг:
Цена: 13168.00 р.
Наличие на складе: Поставка под заказ.

Описание: Bioequivalence and Statistics in Clinical Pharmacology covers the applications and basic elements of the theory of statistical methods in clinical pharmacology. It establishes techniques used in the assessment of bioequivalence and describes the use of statistics in clinical pharmacology studies of safety, ECG monitoring, efficacy, and population pharmacokinetics. The authors demonstrate study design, analysis, and interpretation of data using real data examples. The book emphasizes regulatory applications related to drug development and features a wide range of datasets as well as SAS and SPLUS code available on the Internet.

Handbook Of Bioequivalence Testing

Автор: Niazi Sarfaraz K
Название: Handbook Of Bioequivalence Testing
ISBN: 0849303958 ISBN-13(EAN): 9780849303951
Издательство: Taylor&Francis
Цена: 22968.00 р.
Наличие на складе: Поставка под заказ.

Описание: As the generic pharmaceutical industry continues to grow and thrive, so does the need to conduct efficient and successful bioequivalence studies. In recent years, there have been significant changes to the statistical models for evaluating bioequivalence, and advances in the analytical technology used to detect drug and metabolite levels have made bioequivalence testing more difficult to conduct and summarize. The Handbook of Bioequivalence Testing offers a complete and timely description of every aspect of bioequivalence testing, including worldwide regulatory requirements for filing for approval of generic drugs, applying for a waiver, securing regulatory approval of reports, and obtaining regulatory certification of facilities conducting bioequivalence studies.


ООО "Логосфера " Тел:+7(495) 980-12-10 www.logobook.ru
   В Контакте     В Контакте Мед  Мобильная версия