USP 33 NF 28
Author: United States Pharmacopeial Convention
Publisher:
Published: 2010
Total Pages: 491
ISBN-13: 9781889788883
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The United States Pharmacopeia. The National Formulary
Author:
Publisher:
Published: 2003
Total Pages: 1642
ISBN-13:
DOWNLOAD EBOOKQuality Control and Standardization Of Herbals
Author: Dr. Dillip Kumar Jena
Publisher: Thakur Publication Private Limited
Published: 2021-04-14
Total Pages: 200
ISBN-13: 9390972108
DOWNLOAD EBOOKPurchase the e-Book version of ‘Quality Control and Standardization of Herbals’ for B.Pharm 8th Semester, meticulously aligned with the PCI Syllabus. Published by Thakur Publication, this digital edition offers a comprehensive exploration of advanced instrumentation techniques at your fingertips. Upgrade your learning experience with the convenience and portability of an e-Book. Dive into the world of cutting-edge pharmaceutical instrumentation with ease. Get your copy today and embark on a journey of enhanced understanding.
PHARMACEUTICS
Author: Dr. Suresh Kumar Anu Sharma
Publisher: Kavya Publications
Published: 2024-06-25
Total Pages: 267
ISBN-13: 8119944224
DOWNLOAD EBOOKThis book having authorized "Pharmaceutics" (As Per Pharmacy Council of India, PCI Regulations). This book is anticipated to impart a essential and theoretical knowledge on the art and sciences of different pharmaceutical dosage forms used in pharmaceutical industry and also marketed level. The objective of this delivery System . This book contain the various chapter in the form of units such as: Introduction to pharmacopoeia,historical background and development of profession of pharmacy, packaging material, pharmaceutical aid, unit operations, different dosage forms, manufacturing pharmaceutical plants, Novel Drug delivery System etc. This book is designed according to the pharmacy council of India (PCI) educational programme of diploma courses in pharmacy mainly for D. Pharm students, which specially useful all over India. We sincerely request reader to send their valuable suggestions and positive comments for making improvement in the edition of the book.
Bentley's Textbook of Pharmaceutics - E-Book
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.
Integrated Pharmaceutics
Author: Antoine Al-Achi
Publisher: John Wiley & Sons
Published: 2013-01-22
Total Pages: 1024
ISBN-13: 1118356721
DOWNLOAD EBOOKFocusing on the application of physical pharmacy, drug design, and drug regulations as they relate to produce effective dosage forms for drug delivery, Integrated Pharmaceutics provides a comprehensive picture of pharmaceutical product design, describing the science and art behind the concepts of dosage form development. Combining physical pharmacy, product design, and regulatory affairs issues in a single book, the authors address topics governing drug regulations of United States, European, and Japanese agencies and detail new regulatory guidelines, including quality by design, design space analysis, and blend sample uniformity.
Biomedical Tissue Culture
Author: Luca Ceccherini-Nelli
Publisher: BoD – Books on Demand
Published: 2012-10-17
Total Pages: 252
ISBN-13: 9535107887
DOWNLOAD EBOOKThis book describes many aspects of tissue culture models in an extensive manner. The book includes many topics like, the development of cultural methods to produce massive neuronal syncytial connections and induce their fusion with formation of bi- and multinucleated cells, the applicability in research of cell lines derived from the cultivation of placenta derived cells and cell populations with properties of progenitor/stem cells, the procedures that may be used to regenerate cartilage tissue with appropriate mechanical properties, the improvements made in the use of cell culture for virus isolation, tissue-based models for HCV replication in vitro, cultures to study the pathogenicity of enteropathogenic bacteria, the use of viral DNA and cDNA Array in the diagnosis of respiratory tract infections (RTI) in comparison with routine diagnosis methods.
Vaccine Analysis: Strategies, Principles, and Control
Author: Brian K. Nunnally
Publisher: Springer
Published: 2014-11-27
Total Pages: 669
ISBN-13: 3662450240
DOWNLOAD EBOOKThis book is an indispensable tool for anyone involved in the research, development, or manufacture of new or existing vaccines. It describes a wide array of analytical and quality control technologies for the diverse vaccine modalities. Topics covered include the application of both classical and modern bio-analytical tools; procedures to assure safety and control of cross contamination; consistent biological transition of vaccines from the research laboratory to manufacturing scale; whole infectious attenuated organisms, such as live-attenuated and inactivated whole-cell bacterial vaccines and antiviral vaccines using attenuated or inactivated viruses; principles of viral inactivation and the application of these principles to vaccine development; recombinant DNA approaches to produce modern prophylactic vaccines; bacterial subunit, polysaccharide and glycoconjugate vaccines; combination vaccines that contain multiple antigens as well as regulatory requirements and the hurdles of licensure.
Comprehensive Biotechnology
Author:
Publisher: Newnes
Published: 2011-08-26
Total Pages: 5304
ISBN-13: 0080885047
DOWNLOAD EBOOKThe second edition of Comprehensive Biotechnology, Six Volume Set continues the tradition of the first inclusive work on this dynamic field with up-to-date and essential entries on the principles and practice of biotechnology. The integration of the latest relevant science and industry practice with fundamental biotechnology concepts is presented with entries from internationally recognized world leaders in their given fields. With two volumes covering basic fundamentals, and four volumes of applications, from environmental biotechnology and safety to medical biotechnology and healthcare, this work serves the needs of newcomers as well as established experts combining the latest relevant science and industry practice in a manageable format. It is a multi-authored work, written by experts and vetted by a prestigious advisory board and group of volume editors who are biotechnology innovators and educators with international influence. All six volumes are published at the same time, not as a series; this is not a conventional encyclopedia but a symbiotic integration of brief articles on established topics and longer chapters on new emerging areas. Hyperlinks provide sources of extensive additional related information; material authored and edited by world-renown experts in all aspects of the broad multidisciplinary field of biotechnology Scope and nature of the work are vetted by a prestigious International Advisory Board including three Nobel laureates Each article carries a glossary and a professional summary of the authors indicating their appropriate credentials An extensive index for the entire publication gives a complete list of the many topics treated in the increasingly expanding field
Formulating Poorly Water Soluble Drugs
Author: Robert O. Williams III
Publisher: Springer Science & Business Media
Published: 2011-12-04
Total Pages: 656
ISBN-13: 1461411440
DOWNLOAD EBOOKThis volume is intended to provide the reader with a breadth of understanding regarding the many challenges faced with the formulation of poorly water-soluble drugs as well as in-depth knowledge in the critical areas of development with these compounds. Further, this book is designed to provide practical guidance for overcoming formulation challenges toward the end goal of improving drug therapies with poorly water-soluble drugs. Enhancing solubility via formulation intervention is a unique opportunity in which formulation scientists can enable drug therapies by creating viable medicines from seemingly undeliverable molecules. With the ever increasing number of poorly water-soluble compounds entering development, the role of the formulation scientist is growing in importance. Also, knowledge of the advanced analytical, formulation, and process technologies as well as specific regulatory considerations related to the formulation of these compounds is increasing in value. Ideally, this book will serve as a useful tool in the education of current and future generations of scientists, and in this context contribute toward providing patients with new and better medicines.
