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Perspectives On Bioequivalence Pathways For Drug Product Approval, Dubey, Vaibhav


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Автор: Dubey, Vaibhav
Название:  Perspectives On Bioequivalence Pathways For Drug Product Approval
ISBN: 9780128241417
Издательство: Elsevier Science
Классификация: ISBN-10: 0128241411
Обложка/Формат: Paperback
Вес: 0.00 кг.
Дата издания: 01.08.2021
Язык: English
Ссылка на Издательство: Link
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Поставляется из: Европейский союз
Описание:

Perspectives on Bioequivalence Pathways for Drug Product Approval: Across Dosage Form, Route of Administration and Geographical Jurisdictions explains the role of alternative approaches to bioequivalence across various dosage forms, route of administration, and regulatory bodies with an ultimate aim of reducing clinical trial and bioequivalence study burdens. Sections focus on alternative bioequivalence approaches that can be fostered to minimize human testing, along with instigating new ideas and opening new avenues for the development of such approaches. It will be useful to pharmaceutical scientists working to produce affordable medicines to all as well as regulatory agencies, pharmaceutical companies, formulation scientists and clinical scientists.

This book covers several administration routes and deals with biowaivers for dosage form, routes of administration and geographical jurisdiction. Divided into five sections, including oral drug products, ophthalmic drug products, topical and transdermal drug products, orally inhaled and nasal drug products, and complex injectables, this book includes multiple real-world case studies alongside theory and protocols.




Topical Drug Bioavailability, Bioequivalence, and Penetration

Автор: Vinod P. Shah; Howard I. Maibach; John Jenner
Название: Topical Drug Bioavailability, Bioequivalence, and Penetration
ISBN: 1493938568 ISBN-13(EAN): 9781493938568
Издательство: Springer
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Цена: 18284.00 р.
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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.

Название: Generics and Bioequivalence
ISBN: 0367208326 ISBN-13(EAN): 9780367208325
Издательство: Taylor&Francis
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Цена: 7648.00 р.
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Описание: Published in 1994: This text focuses on the determination of bioequivalence between formulations that are pharmaceutically equivalent and manufactured using acceptable chemistry, manufacturing and controls and in accordance with Good Manufacturing Practices.

Design and Analysis of Bioavailability and Bioequivalence Studies, Third Edition BABE-Solution bundle version

Автор: Chow
Название: Design and Analysis of Bioavailability and Bioequivalence Studies, Third Edition BABE-Solution bundle version
ISBN: 1439813582 ISBN-13(EAN): 9781439813584
Издательство: Taylor&Francis
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Цена: 34605.00 р.
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Описание: Containing four new chapters, along with several new and updated sections, this third edition reviews the latest progress of activities and results in bioavailability and bioequivalence on regulatory requirements, scientific and practical issues, and statistical methodology. It presents the current status of regulations on bioavailability and bioequivalence, including guidelines/guidances issued by the FDA, EMEA, and WHO. This edition addresses frequently asked questions and explores sample size determination, meta-analysis, and pharmacokinetics. It also offers a basic version of PharmaSoftware Solutions, Inc.’s BABE Solution 2008, with bioequivalence assessment for in vivo bioequivalence studies.

Generics and Bioequivalence

Название: Generics and Bioequivalence
ISBN: 0367208318 ISBN-13(EAN): 9780367208318
Издательство: Taylor&Francis
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Цена: 22968.00 р.
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Описание: For over five hundred years, Muslim dynasties ruled parts of northern and central India. Scholars have long drawn upon works written in Persian and Arabic about this epoch, yet they have neglected the many histories that India`s learned elite wrote about Indo-Muslim rule in Sanskrit. Audrey Truschke offers a groundbreaking analysis of these texts.

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.
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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.

Bioequivalence Requirements in Various Global Jurisdictions

Автор: Isadore Kanfer
Название: Bioequivalence Requirements in Various Global Jurisdictions
ISBN: 3319680773 ISBN-13(EAN): 9783319680774
Издательство: Springer
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Цена: 25155.00 р.
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Описание:

Although the Bioequivalence (BE) requirements in many global jurisdictions have much in common, differences in certain approaches and requirements such as definitions and terms, choice of comparator (reference) product, acceptance criteria, fasted and fed studies, single and multi-dose studies, biowaivers and products not intended for absorption into the systemic circulation (locally acting medicines and dosage forms), amongst others, provide food for thought that standardisation should be a high priority objective in order to result in a harmonized international process for the market approval of products using BE. An important objective of Bioequivalence Requirements in Various Global Jurisdictions is to attempt to gather the various BE requirements used in different global jurisdictions to provide a single source of relevant information. This information from, Brazil, Canada, China, European Union, India, Japan, MENA, Russia South Africa, the

USA and WHO will be of value to drug manufacturers, regulatory agencies, pharmaceutical scientists and related health organizations and governments around the world in the quest to harmonize regulatory requirements for the market approval of generic products.

Topical Drug Bioavailability, Bioequivalence, and Penetration

Автор: Vinod P. Shah; Howard I. Maibach; John Jenner
Название: Topical Drug Bioavailability, Bioequivalence, and Penetration
ISBN: 1493912887 ISBN-13(EAN): 9781493912889
Издательство: Springer
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Цена: 22359.00 р.
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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.

Bioequivalence and Statistics in Clinical Pharmacology

Автор: Patterson
Название: Bioequivalence and Statistics in Clinical Pharmacology
ISBN: 1584885300 ISBN-13(EAN): 9781584885306
Издательство: Taylor&Francis
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Цена: 13168.00 р.
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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.

Bioequivalence Requirements in Various Global Jurisdictions

Автор: Isadore Kanfer
Название: Bioequivalence Requirements in Various Global Jurisdictions
ISBN: 3319885421 ISBN-13(EAN): 9783319885421
Издательство: Springer
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Цена: 30745.00 р.
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FDA Bioequivalence Standards

Автор: Lawrence X. Yu; Bing V. Li
Название: FDA Bioequivalence Standards
ISBN: 1493955586 ISBN-13(EAN): 9781493955589
Издательство: Springer
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Цена: 19564.00 р.
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Описание:

.- 1 Bioequivalence History

.- Alex Yu, Duxin Sun, Bing Li, and Lawrence X. Yu

.- 2 Fundamentals of Bioequivalence

.- Mei-Ling Chen

.- 3 Basic Statistical Considerations

.- Fairouz T. Makhlouf, Stella C. Grosser, Donald J. Schuirmann

.- 4 The Effects of Food on Drug Bioavailability and Bioequivalence

.- Wayne I. DeHaven and Dale P. Conner

.- 5 Biowaiver and Biopharmaceutics Classification System

.- Ramana S. Uppoor, Jayabharathi Vaidyanathan, Mehul Mehta, and Lawrence X. Yu

.- 6 Bioequivalence of Highly Variable Drugs

.- Barbara M. Davit and Devvrat T. Patel

.- 7 Partial Area under the Curve: An Additional Pharmacokinetic Metric for Bioavailability and Bioequivalence Assessments

.- Hao Zhu, Ramana Uppoor, Mehul Mehta, and Lawrence X. Yu

.- 8 Bioequivalence for Narrow Therapeutic Index Drugs

.- Wenlei Jiang and Lawrence X. Yu

.- 9 Pharmacodynamic Endpoint-based Bioequivalence Studies

.- Peng Zou and Lawrence X. Yu

.- 10 Clinical Endpoint Bioequivalence Study

.- John R Peters

.- 11 Bioequivalence for Liposomal Drug Products

.- Nan Zheng, Wenlei Jiang, Robert Lionberger, and Lawrence X. Yu

.- 12 Bioequivalence for Drug Products Acting Locally within Gastrointestinal Tract

.- Xiaojian Jiang, Yongsheng Yang, and Ethan Stier

.- 13 Bioequivalence for Topical Drug Products

.- April C. Braddy and Dale P. Conner

.- 14 Bioequivalence for Orally Inhaled and Nasal Drug Products

.- Bhawana Saluja, Bing V. Li and Sau L. Lee

.- 15 Bioequivalence: Modeling and Simulation

.- Xinyuan Zhang and Robert Lionberger

.- 16 Bioanalysis

.- Sriram Subramaniam.

FDA Bioequivalence Standards

Автор: Lawrence X. Yu; Bing V. Li
Название: FDA Bioequivalence Standards
ISBN: 1493912518 ISBN-13(EAN): 9781493912513
Издательство: Springer
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Цена: 25155.00 р.
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Review of the Food and Drug Administration`s Processes to Review Medical Device Submissions Under the Pre-Market Approval and Investigational Device E

Название: Review of the Food and Drug Administration`s Processes to Review Medical Device Submissions Under the Pre-Market Approval and Investigational Device E
ISBN: 1296049132 ISBN-13(EAN): 9781296049133
Издательство: Неизвестно
Цена: 2713.00 р.
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