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Prop Pharmaceutical Calculations Custom
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Book Synopsis PROP - Pharmaceutical Calculations Custom E-Book by : Anthem
Download or read book PROP - Pharmaceutical Calculations Custom E-Book written by Anthem and published by Elsevier Health Sciences. This book was released on 2014-08-07 with total page 582 pages. Available in PDF, EPUB and Kindle. Book excerpt: PROP - Pharmaceutical Calculations Custom E-Book
Book Synopsis PROP - Foundation of Pharmaceutical Care Custom E-Book by : Anthem
Download or read book PROP - Foundation of Pharmaceutical Care Custom E-Book written by Anthem and published by Elsevier Health Sciences. This book was released on 2014-04-25 with total page 510 pages. Available in PDF, EPUB and Kindle. Book excerpt: PROP - Foundation of Pharmaceutical Care Custom E-Book
Book Synopsis Intellectual Property Issues in Nanotechnology by : Chetan Keswani
Download or read book Intellectual Property Issues in Nanotechnology written by Chetan Keswani and published by CRC Press. This book was released on 2020-09-08 with total page 395 pages. Available in PDF, EPUB and Kindle. Book excerpt: Intellectual Property Issues in Nanotechnology focuses on the integrated approach for sustained innovation in various areas of nanotechnology. The theme of this book draws to a great extent on the industrial and socio-legal implications of intellectual property rights for nanotechnology-based advances. The book takes a comprehensive look not only at the role of intellectual property rights in omics-based research but also at the ethical and intellectual standards and how these can be developed for sustained innovation. This book attempts to collate and organize information on current attitudes and policies in several emerging areas of nanotechnology. Adopting a unique approach, this book integrates science and business for an inside view of the industry. Peering behind the scenes, it provides a thorough analysis of the foundations of the present day industry for students and professionals alike.
Author :Dr. Anasuya Patil, Dr. Nayyar Parvez, Dr. Sachinkumar Dnyaneshwar Gunjal, Prof. Madhusmruti Khandai, Dr. Rajni Arora, Nagam Santhi Priya Publisher :Shashwat Publication ISBN 13 :8119281233 Total Pages :454 pages Book Rating :4.1/5 (192 download)
Book Synopsis TEXTBOOK ON PHARMACEUTICAL INTELLECTUAL PROPERTY RIGHTS by : Dr. Anasuya Patil, Dr. Nayyar Parvez, Dr. Sachinkumar Dnyaneshwar Gunjal, Prof. Madhusmruti Khandai, Dr. Rajni Arora, Nagam Santhi Priya
Download or read book TEXTBOOK ON PHARMACEUTICAL INTELLECTUAL PROPERTY RIGHTS written by Dr. Anasuya Patil, Dr. Nayyar Parvez, Dr. Sachinkumar Dnyaneshwar Gunjal, Prof. Madhusmruti Khandai, Dr. Rajni Arora, Nagam Santhi Priya and published by Shashwat Publication. This book was released on 2023-08-04 with total page 454 pages. Available in PDF, EPUB and Kindle. Book excerpt: The laws and regulations governing the pharmaceutical industry were adopted to protect the consuming public by attempting to provide drugs of constituent quality, purity, and efficacy. The Food, Drug and Cosmetic Act (the Act) is a living document in that it is amended frequently and interpreted constantly. The act may be imperfect, but careful attention to its provisions plus an effort of good faith by all persons concerned with drug manufacturing can produce the type of product for which the Act and its regulations strives. Even though the applicable laws and regulations may change with regard to specifics, there are, nonetheless, many constant applicable generally. This book serves an overview of the more significant laws, regulations and Acts. This text book describes the Food, Drug and Cosmetic Act, treats briefly regulations bearing on pharmaceutical manufacturing, looks at the structure, powers, and duties of the Food and Drug administration (FDA), describes state and local laws and regulations, and finally, covers the protection of industrial property and product liability.
Book Synopsis Chemoinformatics and Bioinformatics in the Pharmaceutical Sciences by : Navneet Sharma
Download or read book Chemoinformatics and Bioinformatics in the Pharmaceutical Sciences written by Navneet Sharma and published by Academic Press. This book was released on 2021-05-21 with total page 514 pages. Available in PDF, EPUB and Kindle. Book excerpt: Chemoinformatics and Bioinformatics in the Pharmaceutical Sciences brings together two very important fields in pharmaceutical sciences that have been mostly seen as diverging from each other: chemoinformatics and bioinformatics. As developing drugs is an expensive and lengthy process, technology can improve the cost, efficiency and speed at which new drugs can be discovered and tested. This book presents some of the growing advancements of technology in the field of drug development and how the computational approaches explained here can reduce the financial and experimental burden of the drug discovery process. This book will be useful to pharmaceutical science researchers and students who need basic knowledge of computational techniques relevant to their projects. Bioscientists, bioinformaticians, computational scientists, and other stakeholders from industry and academia will also find this book helpful. - Provides practical information on how to choose and use appropriate computational tools - Presents the wide, intersecting fields of chemo-bio-informatics in an easily-accessible format - Explores the fundamentals of the emerging field of chemoinformatics and bioinformatics
Book Synopsis Intellectual Property Rights in Pharmaceutical Test Data by : Adam Buick
Download or read book Intellectual Property Rights in Pharmaceutical Test Data written by Adam Buick and published by Springer Nature. This book was released on 2023-05-12 with total page 236 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book considers the intellectual property protection of clinical test data that has been submitted to governments, in particular through test data exclusivity rights. It focuses on how these intellectual property rights first emerged in the early 1980s, how they have globalised over the past four decades, and what impact they have had upon access to medicine. This book makes a number of significant and original contributions to the literature around the protection of submitted test data. First, the book draws upon the theory of regulatory globalisation to provide an explanation of how intellectual property rights in submitted pharmaceutical test data have become nearly ubiquitous in the legal systems of most major economies. Second, through a comprehensive analysis and synthesis of provisions on the protection of submitted test data in free trade agreements, as well as a comparison of a range of national approaches to the protection of submitted test data, it reveals the broader global regulatory pattern that has given rise to these intellectual property rights. Third, by analysing data on drug approvals in the US, it provides an empirical insight into the impact of test data exclusivity in national pharmaceutical markets. Fourth, the book covers a number of developments regarding test data exclusivity that have occurred as a result of responses to the COVID-19 pandemic, both at the national level as well as at the World Trade Organisation (WTO). This book will appeal to academics researching the intersection of intellectual property and the life sciences, civil society activists working to promote access to medicines, and students (particularly those at the post-graduate level) studying the relationship between intellectual property and medicine.
Book Synopsis Subject List of Works on the Laws of Industrial Property (patents, Designs and Trade Marks) and Copyright by : Great Britain. Patent Office. Library
Download or read book Subject List of Works on the Laws of Industrial Property (patents, Designs and Trade Marks) and Copyright written by Great Britain. Patent Office. Library and published by . This book was released on 1909 with total page 96 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Teach Yourself the Basics of Aspen Plus by : Ralph Schefflan
Download or read book Teach Yourself the Basics of Aspen Plus written by Ralph Schefflan and published by John Wiley & Sons. This book was released on 2016-09-13 with total page 284 pages. Available in PDF, EPUB and Kindle. Book excerpt: The complete step-by-step guide to mastering the basics of Aspen Plus software Used for a wide variety of important scientific tasks, Aspen Plus software is a modeling tool used for conceptual design, optimization, and performance monitoring of chemical processes. After more than twenty years, it remains one of the most popular and powerful chemical engineering programs used both industrially and academically. Teach Yourself the Basics of Aspen Plus, Second Edition continues to deliver important fundamentals on using Aspen Plus software. The new edition focuses on the newest version of Aspen Plus and covers the newest functionalities. Lecture-style chapters set the tone for maximizing the learning experience by presenting material in a manner that emulates an actual workshop classroom environment. Important points are emphasized through encouragement of hands-on learning techniques that direct learners toward achievement in creating effective designs fluidly and with confidence. Teach Yourself the Basics of Aspen Plus, Second Edition includes: Examples embedded within the text to focus the reader on specific aspects of the material being covered Workshops at the end of each chapter that provide opportunities to test the reader's knowledge in that chapter's subject matter Functionalities covered in the newest version of Aspen including the solution of a flowsheet by an equation oriented, EO approach, and the solution of problems which involve electrolyte equilibria Aspen Plus executable format as well as .txt format files containing details of the examples and the workshops as well as their solutions are provided as a download Designed with both students and professionals in mind, Teach Yourself the Basics of Aspen Plus, Second Edition is like having a personal professor 24/7. Its revolutionary format is an exciting way to learn how to operate this highly sophisticated software—and a surefire way for readers to get the results they expect.
Book Synopsis Forgotten Intellectual Property Lore by : Shubha Ghosh
Download or read book Forgotten Intellectual Property Lore written by Shubha Ghosh and published by Edward Elgar Publishing. This book was released on 2020-10-30 with total page 448 pages. Available in PDF, EPUB and Kindle. Book excerpt: This innovative book explores forgotten disputes over intellectual property and the ways in which creative people and sovereigns have managed these disputes throughout the centuries. With a focus on reform, it raises important questions about the resilience of legal rules and challenges the methodology behind traditional legal analyses. Focusing on lore and traditions, expert contributors incorporate contextual understandings that are rooted in history, sociology, political science, and literary studies into their analyses.
Book Synopsis Pharmaceutical Calculations by : Mitchell J. Stoklosa
Download or read book Pharmaceutical Calculations written by Mitchell J. Stoklosa and published by . This book was released on 1986 with total page 428 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Intellectual Property Damages by : Mark A. Glick
Download or read book Intellectual Property Damages written by Mark A. Glick and published by John Wiley & Sons. This book was released on 2002-12-30 with total page 504 pages. Available in PDF, EPUB and Kindle. Book excerpt: A comprehensive resource for anyone involved in intellectualproperty litigation With Intellectual Property Damages you'll get the basics of theintellectual property litigation process, the essential "rules" inpostulating damages theories, the basics of IP law, the economicpolicies that are the foundation for much of IP litigation, theskills necessary to correctly calculate damages in IP cases--andmore! Order your copy today!
Book Synopsis Burger's Medicinal Chemistry, Drug Discovery and Development, 8 Volume Set by :
Download or read book Burger's Medicinal Chemistry, Drug Discovery and Development, 8 Volume Set written by and published by John Wiley & Sons. This book was released on 2021-04-20 with total page 6057 pages. Available in PDF, EPUB and Kindle. Book excerpt: Burger’s Medicinal Chemistry, Drug Discovery and Development Explore the freshly updated flagship reference for medicinal chemists and pharmaceutical professionals The newly revised eighth edition of the eight-volume Burger’s Medicinal Chemistry, Drug Discovery and Development is the latest installment in this celebrated series covering the entirety of the drug development and discovery process. With the addition of expert editors in each subject area, this eight-volume set adds 35 chapters to the extensive existing chapters. New additions include analyses of opioid addiction treatments, antibody and gene therapy for cancer, blood-brain barrier, HIV treatments, and industrial-academic collaboration structures. Along with the incorporation of practical material on drug hunting, the set features sections on drug discovery, drug development, cardiovascular diseases, metabolic diseases, immunology, cancer, anti-Infectives, and CNS disorders. The text continues the legacy of previous volumes in the series by providing recognized, renowned, authoritative, and comprehensive information in the area of drug discovery and development while adding cutting-edge new material on issues like the use of artificial intelligence in medicinal chemistry. Included: Volume 1: Methods in Drug Discovery, edited by Kent D. Stewart Volume 2: Discovering Lead Molecules, edited by Kent D. Stewart Volume 3: Drug Development, edited by Ramnarayan S. Randad and Michael Myers Volume 4: Cardiovascular, Endocrine, and Metabolic Diseases, edited by Scott D. Edmondson Volume 5: Pulmonary, Bone, Immunology, Vitamins, and Autocoid Therapeutic Agents, edited by Bryan H. Norman Volume 6: Cancer, edited by Barry Gold and Donna M. Huryn Volume 7: Anti-Infectives, edited by Roland E. Dolle Volume 8: CNS Disorders, edited by Richard A. Glennon Perfect for research departments in the pharmaceutical and biotechnology industries, Burger’s Medicinal Chemistry, Drug Discovery and Development can be used by graduate students seeking a one-stop reference for drug development and discovery and deserves its place in the libraries of biomedical research institutes, medical, pharmaceutical, and veterinary schools.
Book Synopsis Treasury Decisions Under Customs and Other Laws by : United States. Dept. of the Treasury
Download or read book Treasury Decisions Under Customs and Other Laws written by United States. Dept. of the Treasury and published by . This book was released on 1921 with total page 680 pages. Available in PDF, EPUB and Kindle. Book excerpt: Vols. for 1904-1926 include also decisions of the United States Board of General Appraisers.
Book Synopsis Intellectual Property Enforcement by : Michael Blakeney
Download or read book Intellectual Property Enforcement written by Michael Blakeney and published by Edward Elgar Publishing. This book was released on 2012-01-01 with total page 407 pages. Available in PDF, EPUB and Kindle. Book excerpt: 'Professor Blakeney has written a detailed work on the current state of international enforcement of intellectual property rights. Using the background to, and the negotiation of, the Anti-Counterfeiting Trade Agreement, as well as the provisions of the ACTA itself, the book is a mine of information and analysis. Professor Blakeney's long experience of work on the laws and practice of IPR enforcement as a right-holder, an administrator, and as an academic and researcher, are second to none and it shows in this all-encompassing work.' – John Anderson, Global Anti-Counterfeiting Network This important book is the first detailed analytical treatment of the Anti-Counterfeiting Trade Agreement (ACTA) and its impact on intellectual property enforcement. The ACTA had been formulated to deal with the burgeoning growth in the trade in counterfeit and pirate products which was estimated to have increased ten-fold since the promulgation of the TRIPS Agreement in 1994. The book clarifies how the ACTA supplements the enforcement provisions of the TRIPS Agreement, namely by: expanding the reach of border protection to infringing goods in transit; providing greater detail of the implementation of civil enforcement and; providing for the confiscation of the proceeds of intellectual property crimes. As the book illustrates, a significant additional innovation is the introduction of provisions dealing with enforcement of intellectual property rights in the digital environment. This book will strongly appeal to intellectual property rights policymakers at the World Trade Organization and World Intellectual Property Organization, legal practitioners, academics and students.
Book Synopsis Illicit Trade Trade in Counterfeit Pharmaceutical Products by : OECD
Download or read book Illicit Trade Trade in Counterfeit Pharmaceutical Products written by OECD and published by OECD Publishing. This book was released on 2020-03-23 with total page 94 pages. Available in PDF, EPUB and Kindle. Book excerpt: This report, one in a series of studies by the OECD and the European Union Intellectual Property Office (EUIPO), enhances understanding of the issues and challenges facing governments, businesses and society posed by the trade in fake pharmaceutical products.
Book Synopsis World Trade Information Service by :
Download or read book World Trade Information Service written by and published by . This book was released on 1956 with total page 526 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Pharmaceutical Profiling in Drug Discovery for Lead Selection by : Ronald Borchardt
Download or read book Pharmaceutical Profiling in Drug Discovery for Lead Selection written by Ronald Borchardt and published by Springer Science & Business Media. This book was released on 2005-12-05 with total page 512 pages. Available in PDF, EPUB and Kindle. Book excerpt: At a time when pharmaceutical companies have limited resources to develop newer and better drugs, they must continually evaluate the effectiveness and efficiency of their research and development process. This volume focuses on how to increase the efficiency of drug discovery and development. Written by experienced discovery scientists from diverse disciplines, including chemistry, drug metabolism, and development sciences, it details in silico, in vitro, and in vivo tools for prediction, measurement, and application of compound properties to select and improve potential drug candidates.