Fundamentals Of Biologicals Regulation

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Fundamentals of Biologicals Regulation

Author : Rebecca Sheets
Publisher : Academic Press
ISBN 13 : 0128094435
Total Pages : 450 pages
Book Rating : 4.1/5 (28 download)

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Book Synopsis Fundamentals of Biologicals Regulation by : Rebecca Sheets

Download or read book Fundamentals of Biologicals Regulation written by Rebecca Sheets and published by Academic Press. This book was released on 2017-12-13 with total page 450 pages. Available in PDF, EPUB and Kindle. Book excerpt: Fundamentals of Biologicals Regulation: Vaccines and Biotechnology Medicines serves as an introduction to the international regulatory arena in which biologicals are developed and offers an overview of the processes and insight into the scientific concepts underpinning global regulations. This book will provide multiple levels of readership with guidance on basic concepts, a detailed look at regulatory challenges, and practical insight into how regulators consider regulatory science and regulatory process issues across various regions. With numerous case studies, learning activities, and real-world examples across several classes of biotechnological products, this book is a valuable and comprehensive resource for graduate students, professors, regulatory officials, and industry scientists working with biologicals. Provides a broad overview and introduction to the regulatory processes, from product development pathways, through clinical trials and product development stages and beyond Includes FDA, EMA, ICH, and WHO recommendations and guidelines so readers can compare and contrast the different regulatory regions with their expectations and understand why they are different Contains chapters on some of the exceptions to the process including how biosimilars and in vitro diagnostics are regulated Includes numerous case studies, learning activities, and real-world examples across several classes of biotechnological products

Fundamentals of International Pharmaceutical and Biologics Regulations

Author : Zeeshaan Arshad
Publisher :
ISBN 13 : 9780997769739
Total Pages : 252 pages
Book Rating : 4.7/5 (697 download)

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Book Synopsis Fundamentals of International Pharmaceutical and Biologics Regulations by : Zeeshaan Arshad

Download or read book Fundamentals of International Pharmaceutical and Biologics Regulations written by Zeeshaan Arshad and published by . This book was released on 2017 with total page 252 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Fundamentals of Pharmaceutical and Biologics Regulations, Third Edition

Author : Gloria Hall
Publisher :
ISBN 13 : 9781947493513
Total Pages : pages
Book Rating : 4.4/5 (935 download)

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Book Synopsis Fundamentals of Pharmaceutical and Biologics Regulations, Third Edition by : Gloria Hall

Download or read book Fundamentals of Pharmaceutical and Biologics Regulations, Third Edition written by Gloria Hall and published by . This book was released on 2020-07-29 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:

Fundamentals of Pharmaceutical and Biologics Regulations: a Global Perspective

Author : Regulatory Affairs Professionals Society
Publisher :
ISBN 13 : 9781947493865
Total Pages : 0 pages
Book Rating : 4.4/5 (938 download)

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Book Synopsis Fundamentals of Pharmaceutical and Biologics Regulations: a Global Perspective by : Regulatory Affairs Professionals Society

Download or read book Fundamentals of Pharmaceutical and Biologics Regulations: a Global Perspective written by Regulatory Affairs Professionals Society and published by . This book was released on 2023-05 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Fundamentals of Pharmaceutical and Biologics Regulations

Author : Pamela A. Jones
Publisher :
ISBN 13 : 9781947493315
Total Pages : pages
Book Rating : 4.4/5 (933 download)

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Book Synopsis Fundamentals of Pharmaceutical and Biologics Regulations by : Pamela A. Jones

Download or read book Fundamentals of Pharmaceutical and Biologics Regulations written by Pamela A. Jones and published by . This book was released on 2019 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:

Fundamentals of International Pharmaceutical and Biologics Regulations

Author : Gloria Hall
Publisher :
ISBN 13 : 9781947493216
Total Pages : pages
Book Rating : 4.4/5 (932 download)

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Book Synopsis Fundamentals of International Pharmaceutical and Biologics Regulations by : Gloria Hall

Download or read book Fundamentals of International Pharmaceutical and Biologics Regulations written by Gloria Hall and published by . This book was released on 2018-09-04 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:

Fundamentals of US Regulatory Affairs

Author : Syed Rizwanuddin Ahmad
Publisher :
ISBN 13 : 9780997769777
Total Pages : pages
Book Rating : 4.7/5 (697 download)

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Book Synopsis Fundamentals of US Regulatory Affairs by : Syed Rizwanuddin Ahmad

Download or read book Fundamentals of US Regulatory Affairs written by Syed Rizwanuddin Ahmad and published by . This book was released on 2017-07 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:

Fundamentals of Pharmaceutical and Biologics Regulations, Fourth Edition

Author : Gloria Hall
Publisher :
ISBN 13 : 9781947493698
Total Pages : pages
Book Rating : 4.4/5 (936 download)

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Book Synopsis Fundamentals of Pharmaceutical and Biologics Regulations, Fourth Edition by : Gloria Hall

Download or read book Fundamentals of Pharmaceutical and Biologics Regulations, Fourth Edition written by Gloria Hall and published by . This book was released on 2021-07-23 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:

Fundamentals of US Pharmaceutical and Biologics Regulations

Author : Syed Rizwanuddin Ahmad
Publisher :
ISBN 13 : 9781947493018
Total Pages : pages
Book Rating : 4.4/5 (93 download)

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Book Synopsis Fundamentals of US Pharmaceutical and Biologics Regulations by : Syed Rizwanuddin Ahmad

Download or read book Fundamentals of US Pharmaceutical and Biologics Regulations written by Syed Rizwanuddin Ahmad and published by . This book was released on 2017-08 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: Laws and regulations governing pharmaceutical and biologics products manufacture and marketing in the US.

Global Pharmaceutical and Biologics Regulation

Author :
Publisher :
ISBN 13 : 9780989802864
Total Pages : pages
Book Rating : 4.8/5 (28 download)

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Book Synopsis Global Pharmaceutical and Biologics Regulation by :

Download or read book Global Pharmaceutical and Biologics Regulation written by and published by . This book was released on 2014-05-23 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: Compilation of the pharmaceutical and biologics chapters from Fundamentals of US Regulatory Affairs Eighth Edition and Fundamentals of International Regulatory Affairs Second Edition,

Fundamentals of International Regulatory Affairs, Fifth Edition

Author : Gloria Hall
Publisher :
ISBN 13 : 9781947493636
Total Pages : pages
Book Rating : 4.4/5 (936 download)

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Book Synopsis Fundamentals of International Regulatory Affairs, Fifth Edition by : Gloria Hall

Download or read book Fundamentals of International Regulatory Affairs, Fifth Edition written by Gloria Hall and published by . This book was released on 2021-06-25 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:

Fundamentals of Canadian Regulatory Affairs Fourth Edition

Author : Jamie Austin
Publisher :
ISBN 13 : 9780989802826
Total Pages : pages
Book Rating : 4.8/5 (28 download)

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Book Synopsis Fundamentals of Canadian Regulatory Affairs Fourth Edition by : Jamie Austin

Download or read book Fundamentals of Canadian Regulatory Affairs Fourth Edition written by Jamie Austin and published by . This book was released on 2014-01-05 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: Reference book on the laws and regulations governing healthcare products on the Canadian market.

Regulatory Aspects of Gene Therapy and Cell Therapy Products

Author : Maria Cristina Galli
Publisher : Springer Nature
ISBN 13 : 3031345673
Total Pages : 243 pages
Book Rating : 4.0/5 (313 download)

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Book Synopsis Regulatory Aspects of Gene Therapy and Cell Therapy Products by : Maria Cristina Galli

Download or read book Regulatory Aspects of Gene Therapy and Cell Therapy Products written by Maria Cristina Galli and published by Springer Nature. This book was released on 2023-08-01 with total page 243 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book discusses the different regulatory pathways for Advanced Therapy Medicinal Products implemented by national agencies in North and South America, Europe and Asia and by international bodies in the effort of international harmonization. This book represents an update of the first edition, as it covers regulatory novelties and accumulated experience in the regions already addressed. In addition, this new edition offers a wider international perspective: new chapters are included covering Advanced Therapy Medicinal Products regulations in India, Malaysia, Spain and Thailand, the European Pharmacopoeia texts for gene therapy medicinal products as well as international harmonization programs. Each chapter, authored by experts from various regulatory bodies throughout the international community, walks the reader through the applications of nonclinical research to translational clinical research to licensure and therapeutic use of these innovative products. More specifically, each chapter offers insights into fundamental considerations that are essential for developers of Advanced Therapy Medicinal Products in the areas of product quality, pharmacology and toxicology, clinical trial design and HTA pathways, as well as pertinent ‘must-know’ guidelines and regulations. Regulatory Aspects of Gene Therapy and Cell Therapy Products: a Global Perspective is part of the American Society of Gene & Cell Therapy sub-series of the highly successful Advances in Experimental Medicine and Biology series. It is essential reading for graduate students, clinicians, and researchers interested in gene and cell therapy and the regulation of pharmaceuticals.

Guide to EU Pharmaceutical Regulatory Law

Author : Sally Shorthose
Publisher : Kluwer Law International B.V.
ISBN 13 : 9041170022
Total Pages : 589 pages
Book Rating : 4.0/5 (411 download)

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Book Synopsis Guide to EU Pharmaceutical Regulatory Law by : Sally Shorthose

Download or read book Guide to EU Pharmaceutical Regulatory Law written by Sally Shorthose and published by Kluwer Law International B.V.. This book was released on 2017-02-17 with total page 589 pages. Available in PDF, EPUB and Kindle. Book excerpt: In the European Union (EU) and its Member States, as elsewhere, the marketing of pharmaceuticals has become subject to an increasingly complex web of legislation and regulation, resulting from the intense scrutiny necessary to ensure such essential products are not only efficacious but safe. This useful volume lays out this system with extraordinary clarity and logic. Adopting a Europe-wide perspective on the law governing pharmaceuticals, expert authors from the law firm Bird & Bird LLP map the life cycle of a medicinal product or medical device from development to clinical trials to product launch and ongoing pharmacovigilance, offering comprehensive and unambiguous guidance at every stage. A brief overview of how the proposed exit from the EU by the UK will affect the regulatory regime is also included. Following an introductory overview focusing on the regulatory framework for pharmaceuticals in Europe – from its underlying rationales to the relevant committees and agencies – each of fifteen incisive chapters examines a particular process or subject. Among the many topics and issues covered are the following: - obtaining a marketing authorisation; - stages and standards for creating a product dossier; - clinical trials; - how and when an abridged procedure can be used; - criteria for conditional marketing authorisations; - generic products and ‘essential similarity’; - paediatric use and the requisite additional trials; - biologicals and ‘biosimilars’; - homeopathic and herbal medicines; - reporting procedures; - pharmacovigilance; - parallel trade; - relevant competition law and intellectual property rights; and - advertising. In addition, national variation charts in many of the chapters illustrate eight major jurisdictions (Belgium, France, Germany, Italy, The Netherlands, Spain, Sweden, and the UK). Sample forms and URLs for the most important Directives are included. Pharmaceutical lawyers and regulatory advisers, both in-house and in private practice, will welcome this unique book. It offers immeasurable value for all who need to understand the process of bringing a medicinal product or medical device to market and the continuing rights and obligations.

Biologics, Biosimilars, and Biobetters

Author : Iqbal Ramzan
Publisher : John Wiley & Sons
ISBN 13 : 1119564654
Total Pages : 328 pages
Book Rating : 4.1/5 (195 download)

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Book Synopsis Biologics, Biosimilars, and Biobetters by : Iqbal Ramzan

Download or read book Biologics, Biosimilars, and Biobetters written by Iqbal Ramzan and published by John Wiley & Sons. This book was released on 2021-02-03 with total page 328 pages. Available in PDF, EPUB and Kindle. Book excerpt: A comprehensive primer and reference, this book provides pharmacists and health practitioners the relevant science and policy concepts behind biologics, biosimilars, and biobetters from a practical and clinical perspective. Explains what pharmacists need to discuss the equivalence, efficacy, safety, and risks of biosimilars with physicians, health practitioners, and patients about Guides regulators on pragmatic approaches to dealing with these drugs in the context of rapidly evolving scientific and clinical evidence Balances scientific information on complex drugs with practical information, such as a checklist for pharmacists

Good Laboratory Practice Regulations Management Briefings

Author : United States. Food and Drug Administration
Publisher :
ISBN 13 :
Total Pages : 60 pages
Book Rating : 4.:/5 (31 download)

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Book Synopsis Good Laboratory Practice Regulations Management Briefings by : United States. Food and Drug Administration

Download or read book Good Laboratory Practice Regulations Management Briefings written by United States. Food and Drug Administration and published by . This book was released on 1979 with total page 60 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Fundamentals of Drug Delivery

Author : Heather A. E. Benson
Publisher : John Wiley & Sons
ISBN 13 : 1119769604
Total Pages : 580 pages
Book Rating : 4.1/5 (197 download)

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Book Synopsis Fundamentals of Drug Delivery by : Heather A. E. Benson

Download or read book Fundamentals of Drug Delivery written by Heather A. E. Benson and published by John Wiley & Sons. This book was released on 2021-10-12 with total page 580 pages. Available in PDF, EPUB and Kindle. Book excerpt: A comprehensive guide to the current research, major challenges, and future prospects of controlled drug delivery systems Controlled drug delivery has the potential to significantly improve therapeutic outcomes, increase clinical benefits, and enhance the safety of drugs in a wide range of diseases and health conditions. Fundamentals of Drug Delivery provides comprehensive and up-to-date coverage of the essential principles and processes of modern controlled drug delivery systems. Featuring contributions by respected researchers, clinicians, and pharmaceutical industry professionals, this edited volume reviews the latest research in the field and addresses the many issues central to the development of effective, controlled drug delivery. Divided in three parts, the book begins by introducing the concept of drug delivery and discussing both challenges and opportunities within the rapidly evolving field. The second section presents an in-depth critique of the common administration routes for controlled drug delivery, including delivery through skin, the lungs, and via ocular, nasal, and otic routes. The concluding section summarizes the current state of the field and examines specific issues in drug delivery and advanced delivery technologies, such as the use of nanotechnology in dermal drug delivery and advanced drug delivery systems for biologics. This authoritative resource: Covers each main stage of the drug development process, including selecting pharmaceutical candidates and evaluating their physicochemical characteristics Describes the role and application of mathematical modelling and the influence of drug transporters in pharmacokinetics and drug disposition Details the physiology and barriers to drug delivery for each administration route Presents a historical perspective and a look into the possible future of advanced drug delivery systems Explores nanotechnology and cell-mediated drug delivery, including applications for targeted delivery and toxicological and safety issues Includes comprehensive references and links to the primary literature Edited by a team of of internationally-recognized experts, Fundamentals of Drug Delivery is essential reading for researchers, industrial scientists, and advanced students in all areas of drug delivery including pharmaceutics, pharmaceutical sciences, biomedical engineering, polymer and materials science, and chemical and biochemical engineering.