Download or read book Dietary Supplements of Plant Origin written by Massimo Maffei and published by CRC Press. This book was released on 2003-05-22 with total page 256 pages. Available in PDF, EPUB and Kindle. Book excerpt: Dietary supplements are estimated to be used regularly by almost 60% of the American population, and over 300 million people worldwide. An important and ever-growing portion of this market is in botanical supplements that are derived from natural plants. Natural, however, does not necessarily mean safe, and although plants can provide health-essent
Download or read book Usp38 Nf33 written by United States Pharmacopeial Convention and published by . This book was released on 2014-11-01 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book The United States Pharmacopeia the National Formulary written by and published by . This book was released on 2006 with total page 156 pages. Available in PDF, EPUB and Kindle. Book excerpt: The USP–NF is a combination of two compendia, the United States Pharmacopeia (USP) and the National Formulary (NF). It contains standards for medicines, dosage forms, drug substances, excipients, biologics, compounded preparations, medical devices, dietary supplements, and other therapeutics. The current version of USP–NF standards deemed official by USP are enforceable by the U.S. Food and Drug Administration for medicines manufactured and marketed in the United States.
Download or read book Usp39 Nf34 written by United States Pharmacopeial Convention and published by . This book was released on 2015-11-01 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book A TEXTBOOK OF PHARMACEUTICAL INORGANIC CHEMISTRY BP104T written by Mr. Atul Narsinva Patkar, Dr. CM Jamkhandi, Dr. B. Prathap, Dr. Anand Mundada, Dr. Jannat ul Firdaus and published by Shashwat Publication. This book was released on 2024-09-25 with total page 242 pages. Available in PDF, EPUB and Kindle. Book excerpt: The titled book is A Textbook of PHARMACEUTICAL INORGANIC CHEMISTRY (Theory) (As per PCI regulation). The idea of book originated by authors to convey a combined database for easy understanding of PHARMACEUTICAL INORGANIC CHEMISTRY (Theory). This book is intended to communicate information on inorganic chemistry, to direct tutors and learners regarding fundamental concepts in PHARMACEUTICAL INORGANIC CHEMISTRY (Theory). 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 Pharmaceutical Jurisprudence 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.
Download or read book A Text Book of Pharmaceutics 1 written by Prachi Pandey and published by JEC PUBLICATION. This book was released on with total page 213 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book having entitles “A Text Book of Pharmaceutics-I” (As Per Pharmacy Council of India, PCI Regulations). This text book is designed to impart a fundamental and theoretical knowledge on the art and sciences of various pharmaceutical dosage forms used in pharmaceutical industry as well as marketed level. This Pharmaceutics subjects deals with the various physical and physicochemical properties and their formulations/evaluations. The practice of the subject helps the students to get a better insight into the various areas of formulations research, development and stability studies of pharmaceutical dosage forms. The main objectives of the completion of this course students shall be able to: 01. Known the complete history of pharmacy profession since lastly. 02. Understand the basics of different dosage forms, pharmaceutical incompatibilities and pharmaceutical calculation involving in it. 03. Understand the professional ways to handling the prescriptions. This text book consists the various chapter in the form of units such as: Historical background and development of profession of pharmacy, Dosage forms, prescriptions, posology, pharmaceutical calculations, powders, liquid dosage forms, monophasic and Biphasic liquids, emulsions, suspensions, suppositories, pharmaceutical incompatibilities and semi-solid dosage forms. This book is designed according to the pharmacy council of India (PCI) curriculum of undergraduate courses in pharmacy specially for B. Pharm students, which mainly useful all over India. We sincerely request reader to send their valuable suggestions and constructive comments for making improvement in the text edition of the book. We extend out good wishes to the students and professor and sincerely hope to have the continued support from them and to our other books in future.
Download or read book The United States Pharmacopeia USP 24 Supplement 1 written by and published by . This book was released on 1999 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Generic Drug Product Development written by Leon Shargel and published by CRC Press. This book was released on 2013-10-24 with total page 400 pages. Available in PDF, EPUB and Kindle. Book excerpt: In this era of increased pharmaceutical industry competition, success for generic drug companies is dependent on their ability to manufacture therapeutic-equivalent drug products in an economical and timely manner, while also being cognizant of patent infringement and other legal and regulatory concerns. Generic Drug Product Development: Solid Oral Dosage Forms, Second Edition presents in-depth discussions from more than 30 noted specialists describing the development of generic drug products—from the raw materials to the development of a therapeutic-equivalent drug product to regulatory approval. Major topics discussed include: Active pharmaceutical ingredients Experimental formulation development, including a new section on Quality by Design (QbD) Scale-up Commercial product formulation Quality control and bioequivalence Drug product performance ANDA regulatory process Post-approval changes Post-marketing surveillance Legislative and patent challenges This second edition also contains a new chapter on the relationship between the FDA and the United States Pharmacopeia and in Chapter 4, using specific examples, the application of Quality by Design (QbD) during formulation development is examined.The book is a thorough guide to the development of solid oral generic dosage formulations. This textbook is ideal for the pharmaceutical industry, graduate programs in pharmaceutical sciences, and health professionals working in the area of generic drug development.
Download or read book Supplement to the National Drug Code Directory written by and published by . This book was released on 1976 with total page 208 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Profiles of Drug Substances Excipients and Related Methodology written by Harry G. Brittain and published by Academic Press. This book was released on 2011-09-06 with total page 360 pages. Available in PDF, EPUB and Kindle. Book excerpt: Volumes in this widely revered series present comprehensive reviews of drug substances and additional materials, with critical review chapters that summarize information related to the characterization of drug substances and excipients. This organizational structure meets the needs of the pharmaceutical community and allows for the development of a timely vehicle for publishing review materials on this topic. The scope of the Profiles series encompasses review articles and database compilations that fall within one of the following six broad categories: Physical profiles of drug substances and excipients; Analytical profiles of drug substances and excipients; Drug metabolism and pharmacokinetic profiles of drug substances and excipients; Methodology related to the characterization of drug substances and excipients; Methods of chemical synthesis; and Reviews of the uses and applications for individual drug substances, classes of drug substances, or excipients. - Presents comprehensive reviews covering all aspects of drug development and formulation of drugs - Profiles creatine monohydrate and fexofenadine hydrochloride, as well as five others - Meets the information needs of the drug development community
Download or read book PHARMACEUTICAL INORGANIC CHEMISTRY written by Dr. Anil Kumar Garige and published by JEC PUBLICATION. This book was released on with total page 236 pages. Available in PDF, EPUB and Kindle. Book excerpt: Pharmaceutical Inorganic Chemistry is an ever-evolving field that forms the cornerstone of modern drug discovery, development, and delivery. This book emerges as a comprehensive guide, meticulously crafted to cater to the burgeoning needs of students, researchers, and professionals engaged in pharmaceutical sciences. Authored by a team of dedicated experts – Dr. Anil Kumar Garige, Dr. Rathnakar Reddy Kotha, Dr. Baswaraju Macha, Dr. Vijitha Chandupatla & Mr Ankit Diwan– it amalgamates their collective expertise and experiences to offer a definitive resource in the realm of inorganic chemistry in pharmaceutical applications. Inorganic chemistry plays a pivotal role in drug design, synthesis, formulation, and analysis, with its impact spanning across various facets of pharmaceutical sciences. This book embarks on a journey through the fundamental principles of inorganic chemistry, elucidating its significance in drug stability, bioavailability, and pharmacological activity. From the intricate coordination chemistry of metal complexes to the intricate mechanisms underlying their interaction with biological systems, each chapter unravels the multifaceted aspects of inorganic compounds in pharmacotherapy. As authors, we recognize the dynamic nature of pharmaceutical sciences and acknowledge the continuous evolution in this field. Hence, this book is designed to serve as a dynamic repository, accommodating updates and advancements to ensure its relevance in the ever-changing landscape of pharmaceutical inorganic chemistry.
Download or read book The Stationery Office Agency Catalogue written by Stationery Office (Great Britain) and published by . This book was released on 2000 with total page 272 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Handbook of Modern Pharmaceutical Analysis written by Satinder Ahuja and published by Elsevier. This book was released on 2001-08-02 with total page 587 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book describes the role modern pharmaceutical analysis plays in the development of new drugs. Detailed information is provided as to how the quality of drug products is assured from the point of discovery until the patient uses the drug. Coverage includes state-of-the-art topics such as analytics for combinatorial chemistry and high-throughput screening, formulation development, stability studies, international regulatory aspects and documentation, and future technologies that are likely to impact the field. Emphasis is placed on current, easy-to-follow methods that readers can apply in their laboratories.No book has effectively replaced the very popular text, Pharmaceutical Analysis, that was edited in the 1960s by Tak Higuchi. This book will fill that gap with an up-to-date treatment that is both handy and authoritative.
Download or read book HMSO Agency Catalogue written by Great Britain. Her Majesty's Stationery Office and published by . This book was released on 2001 with total page 320 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Endotoxins written by Kevin L. Williams and published by CRC Press. This book was released on 2007-02-23 with total page 441 pages. Available in PDF, EPUB and Kindle. Book excerpt: This source expertly examines the discovery, biological structure, control, and continued clarification of endotoxin from a parenteral manufacturing perspective, with in-depth discussion of state-of-the-art technologies involving Limulus amebocyte lysate (LAL) such as assay development, automation, depyrogenation. Completely revised and exp
Download or read book Dietary Reference Intakes for Vitamin C Vitamin E Selenium and Carotenoids written by Institute of Medicine and published by National Academies Press. This book was released on 2000-08-27 with total page 530 pages. Available in PDF, EPUB and Kindle. Book excerpt: This volume is the newest release in the authoritative series of quantitative estimates of nutrient intakes to be used for planning and assessing diets for healthy people. Dietary Reference Intakes (DRIs) is the newest framework for an expanded approach developed by U.S. and Canadian scientists. This book discusses in detail the role of vitamin C, vitamin E, selenium, and the carotenoids in human physiology and health. For each nutrient the committee presents what is known about how it functions in the human body, which factors may affect how it works, and how the nutrient may be related to chronic disease. Dietary Reference Intakes provides reference intakes, such as Recommended Dietary Allowances (RDAs), for use in planning nutritionally adequate diets for different groups based on age and gender, along with a new reference intake, the Tolerable Upper Intake Level (UL), designed to assist an individual in knowing how much is "too much" of a nutrient.
