A TEXTBOOK OF ADVANCED BIOPHARMACEUTICS & PHARMACOKINETICS (MPH 202T) PDF Download
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Author: Dr. Ruchi Jain, Mrs. Pooja Anand Mundada, Mr. Vedant Kumar Prajapati, Dr. Sandeep Ashok Marathe, Dr. S B Thirumalesh Naik
Publisher: Shashwat Publication
ISBN: 9360872520
Category : Medical
Languages : en
Pages : 360
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Book Description
Preface The titled book is “A Textbook of ADVANCED BIOPHARMACEUTICS & PHARMACOKINETICS (MPH 202T)” (As per PCI regulation). The idea of book originated by authors to convey a combined database for easy understanding of ADVANCED BIOPHARMACEUTICS & PHARMACOKINETICS. This book is intended to communicate information on novel drug delivery techniques, to direct tutors and learners regarding fundamental concepts in Pharmacology II. The major aim to write this textbook is to provide information in articulate summarized manner to accomplish necessities of undergraduates as per PCI regulation. This volume is designed not only according to curriculum of undergraduate courses in pharmacy by PCI but also to communicate knowledge on ADVANCED BIOPHARMACEUTICS & PHARMACOKINETICS for post graduate learners. We assured this book will be originated very valuable by graduates, post graduates, professors and industrial learners. However any suggestion for further improvement of text are welcome and will be taken due note of.
Author: Dr. Ruchi Jain, Mrs. Pooja Anand Mundada, Mr. Vedant Kumar Prajapati, Dr. Sandeep Ashok Marathe, Dr. S B Thirumalesh Naik
Publisher: Shashwat Publication
ISBN: 9360872520
Category : Medical
Languages : en
Pages : 360
Get Book Here
Book Description
Preface The titled book is “A Textbook of ADVANCED BIOPHARMACEUTICS & PHARMACOKINETICS (MPH 202T)” (As per PCI regulation). The idea of book originated by authors to convey a combined database for easy understanding of ADVANCED BIOPHARMACEUTICS & PHARMACOKINETICS. This book is intended to communicate information on novel drug delivery techniques, to direct tutors and learners regarding fundamental concepts in Pharmacology II. The major aim to write this textbook is to provide information in articulate summarized manner to accomplish necessities of undergraduates as per PCI regulation. This volume is designed not only according to curriculum of undergraduate courses in pharmacy by PCI but also to communicate knowledge on ADVANCED BIOPHARMACEUTICS & PHARMACOKINETICS for post graduate learners. We assured this book will be originated very valuable by graduates, post graduates, professors and industrial learners. However any suggestion for further improvement of text are welcome and will be taken due note of.
Author: Rajesh Krishna
Publisher: Springer Science & Business Media
ISBN: 038772379X
Category : Medical
Languages : en
Pages : 416
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Book Description
The highly experienced authors here present readers with step-wise, detail-conscious information to develop quality pharmaceuticals. The book is made up of carefully crafted sections introducing key concepts and advances in the areas of dissolution, BA/BE, BCS, IVIC, and product quality. It provides a specific focus on the integration of regulatory considerations and includes case histories highlighting the biopharmaceutics strategies adopted in development of successful drugs.
Author: Milo Gibaldi
Publisher:
ISBN:
Category : Medical
Languages : en
Pages : 196
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Book Description
Author: Sean Ekins
Publisher: John Wiley & Sons
ISBN: 0470037229
Category : Medical
Languages : en
Pages : 840
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Book Description
A unique, holistic approach covering all functions and phases of pharmaceutical research and development While there are a number of texts dedicated to individual aspects of pharmaceutical research and development, this unique contributed work takes a holistic and integrative approach to the use of computers in all phases of drug discovery, development, and marketing. It explains how applications are used at various stages, including bioinformatics, data mining, predicting human response to drugs, and high-throughput screening. By providing a comprehensive view, the book offers readers a unique framework and systems perspective from which they can devise strategies to thoroughly exploit the use of computers in their organizations during all phases of the discovery and development process. Chapters are organized into the following sections: * Computers in pharmaceutical research and development: a general overview * Understanding diseases: mining complex systems for knowledge * Scientific information handling and enhancing productivity * Computers in drug discovery * Computers in preclinical development * Computers in development decision making, economics, and market analysis * Computers in clinical development * Future applications and future development Each chapter is written by one or more leading experts in the field and carefully edited to ensure a consistent structure and approach throughout the book. Figures are used extensively to illustrate complex concepts and multifaceted processes. References are provided in each chapter to enable readers to continue investigating a particular topic in depth. Finally, tables of software resources are provided in many of the chapters. This is essential reading for IT professionals and scientists in the pharmaceutical industry as well as researchers involved in informatics and ADMET, drug discovery, and technology development. The book's cross-functional, all-phases approach provides a unique opportunity for a holistic analysis and assessment of computer applications in pharmaceutics.
Author: Jelena Duris
Publisher: Elsevier
ISBN: 0443186561
Category : Medical
Languages : en
Pages : 340
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Book Description
Computer-Aided Applications in Pharmaceutical Technology: Delivery Systems, Dosage Forms, and Pharmaceutical Unit Operations, Second Edition covers the fundamentals of experimental design application and interpretation in pharmaceutical technology, chemometric methods with an emphasis on their applications in process control, neural computing, data science, computer-aided biopharmaceutical characterization, as well as the application of computational fluid dynamics in pharmaceutical technology. Completely updated, the book introduces the theory and practice of computational tools through new case studies. Chapters cover Quality by Design in pharmaceutical development, overview data mining methodologies, present computer-aided formulation development, cover experimental design applications, and much more. - Presents a comprehensive review of the current state of the art on various computer-aided applications in pharmaceutical technology - Includes case studies to facilitate understanding of various concepts in computer-aided applications - Covers applications such as the development of dosage forms and/or delivery systems, pharmaceutical unit operations, and relevant physiologically based pharmacokinetic simulations
Author: John G. Wagner
Publisher: American Pharmaceutical Association
ISBN:
Category : Medical
Languages : en
Pages : 398
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Book Description
Author: Gianfranco Pasut
Publisher: Elsevier
ISBN: 0444640827
Category : Technology & Engineering
Languages : en
Pages : 514
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Book Description
Polymer–Protein Conjugates: From Pegylation and Beyond helps researchers by offering a unique reference and guide into this fascinating area. Sections cover the challenges surrounding the homogeneity of conjugates, their purity and polymer toxicity on long-term use, and how to deal with the risk of immunogenicity. These discussions help researchers design new projects by taking into account the latest innovations for safe and site selective polymer conjugation to proteins. PEG has been the gold standard and likely will play this role for many years, but alternatives are coming into the market, some of which have already been launched. After five decades of improvements, the ideas in this book are entering into a new era of innovation because of the advances in genetic engineering, biochemistry and a better understanding of the results from clinical use of PEG conjugates in humans. - Provides an overview on the state-of-the-art of protein polymer conjugation - Presents both the pros and cons of polymer-protein conjugates from the point-of-view of their clinical outcomes - Outlines advantages and potential risks of present technology based on PEG - Offers new alternatives for PEG and new approaches for on site-selective protein modification - Identifies future direction of research in this field
Author: Ira R. Berry
Publisher: CRC Press
ISBN: 1040177972
Category : Medical
Languages : en
Pages : 492
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Book Description
This Second Edition examines the mechanisms and means to establish regulatory compliance for pharmaceutical products and company practices. It focuses on major legislative revisions that impact requirements for drug safety reviews, product regulatory approvals, and marketing practices. Written by top industry professionals, practicing attorneys, an
Author: N. K. Jain
Publisher: CBS Publishers & Distributors Pvt Limited, India
ISBN: 9788123905174
Category : Medical
Languages : en
Pages : 406
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Book Description
This book gathers together the research work of leading Indian scientists actually engaged in pharmaceutical research. The contributors are all distinguished experts in their respective fields. All the contributors are scientists working in Indian laboratories, however their achievements in the field are full of valuable information supplemented with adequate references which help the intended readers in digging out the complete information on any aspect. The book has 17 chapters, 150 figures and over 2150 references and will be of immense use for all pharmaceutical industries, RD laboratories, research scientists in universities colleges, teachers as well as post-graduate and graduate students.
Author: D. Nally Joseph
Publisher: CRC Press
ISBN: 0824741935
Category : Medical
Languages : en
Pages : 752
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Book Description
Highlighting key issues and differences among GMPs of Europe, Canada, and the WHO, this reference examines US law and governmental policy affecting domestic and multinational pharmaceutical manufacturing. The book recommend pragmatic ways to interpret and comply with FDA CGMP regulation and related criteria. They focus on geographical redistribution of manufacturing facilities, accommodation of a diversity of regulatory and statutory governance, adaptation to disparate human resources, and new growth areas of manufacture and distribution of homeopathic remedies and dietary supplements, in addition to the greater quality control required of pharmacists and other authorized dispensers.
