Download or read book British Pharmacopoeia Veterinary written by and published by . This book was released on 2008 with total page 388 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book British Pharmacopoeia Veterinary Main 1993 written by HMSO Books and published by Stationery Office Books (TSO). This book was released on 1993 with total page 220 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book The British Pharmacopoeia 1864 to 2014 written by Anthony C. Cartwright and published by Routledge. This book was released on 2016-03-09 with total page 266 pages. Available in PDF, EPUB and Kindle. Book excerpt: The British Pharmacopoeia has provided official standards for the quality of substances, medicinal products and articles used in medicine since its first publication in 1864. It is used in over 100 countries and remains an essential global reference in pharmaceutical research and development and quality control. This book explores how these standards have been achieved through a comprehensive review of the history and development of the pharmacopoeias in the UK, from the early London, Edinburgh and Dublin national pharmacopoeias to the creation of the British Pharmacopoeia and its evolution over 150 years. Trade in medicinal substances and products has always been global, and the British Pharmacopoeia is placed in its global context as an instrument of the British Empire as it first sought to cover the needs of countries such as India and latterly as part of its role in international harmonisation of standards in Europe and elsewhere. The changing contents of the pharmacopoeias over this period reflect the changes in medical practice and the development of dosage forms from products dispensed by pharmacists to commercially manufactured products, from tinctures to the latest monoclonal antibody products. The book will be of equal value to historians of medicine and pharmacy as to practitioners of medicine, pharmacy and pharmaceutical analytical chemistry.
Download or read book Dosage Forms Formulation Developments and Regulations written by Amit Kumar Nayak and published by Elsevier. This book was released on 2023-12-09 with total page 759 pages. Available in PDF, EPUB and Kindle. Book excerpt: Dosage Forms, Formulation Developments and Regulations, Volume One in the Recent and Future Trends in Pharmaceutics series, explores aspects of pharmaceutics, with an original approach focused on technology, novelties and future trends in the field. The book discusses the most recent developments in pharmaceutical preformulation and formulation studies, biopharmaceutics and novel pharmaceutical formulations, regulatory affairs, and good manufacturing practices. Exciting areas such as formulation strategies, optimization techniques, the biopharmaceutical classification system, and pharmaceutical aerosols are included. The field of pharmaceutics is highly dynamic and rapidly expanding day-by-day, so it demands a variety of amplified efforts for designing and developing pharmaceutical processes and formulation strategies. This is an essential reference for researchers in academia and industry as well as advanced graduate students in pharmaceutics. - Examines trends and recent technologies in dosage, formulation and regulation - Contains contributions from leading experts in academia, research, industry and regulatory agencies - Includes high-quality illustrations, flow charts and tables for easy understanding of concepts - Discusses practical examples and research case studies
Download or read book The Veterinarian written by and published by . This book was released on 1858 with total page 748 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Bentley s Textbook of Pharmaceutics E Book written by Sanjay Kumar Jain and published by Elsevier Health Sciences. This book was released on 2011-08-23 with total page 778 pages. Available in PDF, EPUB and Kindle. Book excerpt: This 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.
Download or read book Pharmaceutics GPAT Books Study Notes 7 in 1 Books with 2500 Question Answer As Per Updated Syllabus written by DIWAKAR EDUCATION HUB and published by DIWAKAR EDUCATION HUB. This book was released on 2022-04-01 with total page 1428 pages. Available in PDF, EPUB and Kindle. Book excerpt: Pharmaceutics [GPAT] – Books [Study Notes] 7 Books with 2500+ Question Answer As Per Updated Syllabus Design by Expert Faculties for Secure 152 Marks in Graduate Pharmacy Aptitude Test [ Asked 38 MCQ in Exam] Highlights of Books – As Per Updated Syllabus Graduate Pharmacy Aptitude Test 7 Booklets theory + MCQ In Each Book given 4 Chapters in Details [Total 28] Covered all 28 Chapters – Ex Pharmacy Profession & Introduction to Pharmaceuticals, Introduction to dosage form, Sources of drug information Total 2500 + Questions Answer [ Numerical with Explanation] Design by Pharma Professor & Topper Qualified Students Total 7 Booklets For Secured 152 Marks in Exam For More Details Call/Whats App -7310762592,7078549303
Download or read book British Pharmacopoeia 2003 written by British Pharmacopoeia Commission and published by . This book was released on 2003 with total page 736 pages. Available in PDF, EPUB and Kindle. Book excerpt: This three volume collection with CD-ROM contains the authoritative standard reference for medicines in the United Kingdom. It provides information on the quality of substances used throughout medicine and pharmaceutics. Two volumes contain the Pharmacopoeia while a third volume presents British Pharmacopoeia (Veterinary).
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 A TextBook On Pharmaceutical Inorganic Chemistry written by Mukesh Kumar Bhardwaj and published by Blue Rose Publishers. This book was released on 2022-07-11 with total page 172 pages. Available in PDF, EPUB and Kindle. Book excerpt: We feel pleasure to introduce the first edition of this text-book, covering the subject to the Pharmaceutical Inorganic Chemistry-I prescribed in the first year of bachelor of Pharmacy as per Education Regulation, 2020. The matter has been divided into 8 chapters. Each chapter has been written in some detail in order to prepare the students for the better understanding of the subject of Pharmaceutical Inorganic Chemistry as it is places in the beginning of the course and the newly admitted students may find difficult to understand. This book is in very easily understandable English where students do not find it difficult to understand. This books also helps in clear basic concepts of pharmaceutical inorganic chemistry where students are able to connect the subject with its application in daily life. For preparing the subject, we have consulted the number of books and Indian Pharmacopoeia. I am thankful to the author of them.
Download or read book The Law on Medicines written by H.S. Harrison and published by Springer Science & Business Media. This book was released on 2012-12-06 with total page 544 pages. Available in PDF, EPUB and Kindle. Book excerpt: The Medicines Act 1968 together with its delegated legislation comprehensively controls the manufacture, packaging, labelling, distribution and promotion of medicines for both human and animal use in the United Kingdom. It also controls the import and export of such medicines. It replaced a patchwork of controls which evolved over a century. Since its enactment, more than 150 items of delegated legislation (orders and regulations) have been made under its provisions and about 130 are still operative. The sheer physical bulk of this mass of material causes difficulty, not only in comprehension but also in finding the detail so often required. The situation is exacerbated by the fact that some pieces of legislation have been amended several times. My principal aim is to provide a reference book which contains all of the provisions of the Act and its various orders, regulations as amended to date. The material is arranged to facilitate the search for detail. In order to assist the reader in finding his way through this maze, Chaper 1 consists of a survey of the situation which existed before the Act came into being, together with a synopsis of the present controls. This should enable the reader to appreciate the changes which have occurred and how the system works.
Download or read book Government Publications written by Great Britain. Her Majesty's Stationery Office and published by . This book was released on 1994 with total page 132 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book The Stationery Office Annual Catalogue written by Stationery Office (Great Britain) and published by . This book was released on 2016 with total page 304 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book The Stationery Office Annual Catalogue 2008 written by U K Stationery Office and published by Stationery Office Annual Catal. This book was released on 2009-11 with total page 612 pages. Available in PDF, EPUB and Kindle. Book excerpt: No public library discount on this title.
Download or read book The Veterinary Record written by and published by . This book was released on 1939 with total page 986 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book British Pharmacopoeia 2008 written by British Pharmacopoeia Commission and published by Stationary Office (U.K.). This book was released on 2007 with total page 1230 pages. Available in PDF, EPUB and Kindle. Book excerpt: Contents of package: British pharmacopoeia 2008 (4 vols.) + British pharmacopoeia (veterinary) 2008 (1 vol.) + 1 CD-ROM. Purchase of the BP provides licensed access to the BP 2008 CD-ROM and Online Web Portal on a named single-user basis (the CD is the complete edition, available on request - visit www.pharmacopoeia.org.uk. where purchasers of the BP need to register their proof of purchase) + British pharmacopoeia chemical reference substances catalogue 2007-2008 (18p.). BP 2008 incorporates all the monographs and requirements of the 5th edition of the European pharmacopoeia 2004 as amended by supplements 5.1 to 5.8. Effective date: 1 January 2008 (when it supersedes the 2007 edition, ISBN 9780113227259 and the electronic addendum in 2007). Although published in 2007 this edition carries the year 2008, more accurately reflecting the period for which it is effective. Orders from USA, South Africa, Germany, Switzerland and Austria should be directed to TSO Sales (020 7873 8211)
Download or read book Specification of Drug Substances and Products written by Christopher M. Riley and published by Elsevier. This book was released on 2024-09-22 with total page 910 pages. Available in PDF, EPUB and Kindle. Book excerpt: Specification of Drug Substances and Drug Products is a fully comprehensive reference on Specification Setting for Pharmaceuticals. There have been several recent developments in the ICH Guidelines, which were not captured in previous editions, notably the new guideline on Development of Analytical Procedure and the revisions to the validation guidelines, and the specification guidelines. This edition contains chapters discussing the unique requirements for the universal critical quality attributes, as well as the specific tests required to characterize and control different types of products, ranging in complexity from small molecules in immediate release oral dosage forms to complex products such as drug-antibody conjugates and mRNA-based products. This substantially expanded revision of the 2nd edition will serve as practical comprehensive reference for scientists, managers, educators, and consultants involved in the development and regulation of pharmaceutical products - Presents critical assessment, potential impact, and application of the recent revisions to ICH guidelines on method validation (Q2) (as well as the latest guideline on Analytical Method Development (Q14), and the special regional requirements in non-ICH regions. - Addresses comprehensive treatment of the development and validation of analytical methodologies used in the analysis, control, and specification of a variety of different types of dosage forms, ranging from traditional oral solid dosage forms to proteins, nRNA-based drugs, vaccines, and gene therapy. This book will also address drug–device combination products such as digital drug delivery systems, transdermal systems, and inhalation products. - Presents detailed treatment of latest statistical approaches, including new approaches to the treatment of validation data method, specification setting, and shelf-life prediction (based on stability data).
