Books in Pharmaceutical technology

21-30 of 54 results in All results

The Future of Pharmaceutical Product Development and Research

• 1st Edition
• August 19, 2020
• Rakesh Kumar Tekade
• English
• Hardback 978-0-12-814455-8

  9 7 8 - 0 - 1 2 - 8 1 4 4 5 5 - 8
• eBook 978-0-12-814456-5

  9 7 8 - 0 - 1 2 - 8 1 4 4 5 6 - 5

The Future of Pharmaceutical Product Development and Research examines the latest developments in the pharmaceutical sciences, also highlighting key developments, research and future opportunities. Written by experts in the field, this volume in the Advances in Pharmaceutical Product Development and Research series deepens our understanding of the product development phase of drug discovery and drug development. Each chapter covers fundamental principles, advanced methodologies and technologies employed by pharmaceutical scientists, researchers and the pharmaceutical industry. The book focuses on excipients, radiopharmaceuticals, and how manufacturing should be conducted in an environment that follows Good Manufacturing Practice (GMP) guidelines. Researchers and students will find this book to be a comprehensive resource for those working in, and studying, pharmaceuticals, cosmetics, biotechnology, foods and related industries.

Transdermal Drug Delivery

• 1st Edition
• June 9, 2020
• Kevin Ita
• English
• Paperback 978-0-12-822550-9

  9 7 8 - 0 - 1 2 - 8 2 2 5 5 0 - 9
• eBook 978-0-12-822551-6

  9 7 8 - 0 - 1 2 - 8 2 2 5 5 1 - 6

Transdermal Drug Delivery: Concepts and Application provides comprehensive background knowledge and documents the most recent advances made in the field of transdermal drug delivery. It provides comprehensive and updated information regarding most technologies and formulation strategies used for transdermal drug delivery. There has been recent growth in the number of research articles, reviews, and other types of publications in the field of transdermal drug delivery. Research in this area is active both in the academic and industry settings. Ironically, only about 40 transdermal products with distinct active pharmaceutical ingredients are in the market indicating that more needs to be done to chronicle recent advances made in this area and to elucidate the mechanisms involved. This book will be helpful to researchers in the pharmaceutical and biotechnological industries as well as academics and graduate students working in the field of transdermal drug delivery and professionals working in the field of regulatory affairs focusing on topical and transdermal drug delivery systems. Researchers in the cosmetic and cosmeceutical industries, as well as those in chemical and biological engineering, will also find this book useful.

Mosby's Sterile Compounding for Pharmacy Technicians

• 2nd Edition
• December 1, 2019
• Karen Davis
• English
• Paperback 978-0-323-67324-2

  9 7 8 - 0 - 3 2 3 - 6 7 3 2 4 - 2
• eBook 978-0-323-70981-1

  9 7 8 - 0 - 3 2 3 - 7 0 9 8 1 - 1

Gain a complete introduction to institutional pharmacy practice and efficiently prepare for the new sterile compounding certification exam! Comprehensively covering sterile products, aseptic technique, and the workings of the sterile compounding facility, Mosby’s Sterile Compounding for Pharmacy Technicians: Principles and Practice, 2nd Edition, focuses on safe and accurate practice. This edition has expanded and updated coverage to address preparation, processing, medications, technique, and documentation, with review, analysis, and application of <USP 797>, <USP 800>, and <USP 825> and additional content on waste management, workflow, safety and compliance, billing and reimbursement, and emergency management. Illustrations abound, and content is brought to life with an updated art program, step-by-step procedures, and technician notes and alerts. Certification review questions are included with each chapter, and online student and instructor resources round out the offering.

Principles of Parenteral Solution Validation

• 1st Edition
• November 27, 2019
• Igor Gorsky + 1 more
• English
• Paperback 978-0-12-809412-9

  9 7 8 - 0 - 1 2 - 8 0 9 4 1 2 - 9
• eBook 978-0-12-809446-4

  9 7 8 - 0 - 1 2 - 8 0 9 4 4 6 - 4

Principles of Parenteral Solution Validation: A Practical Lifecycle Approach covers all aspects involved in the development and process validation of a parenteral product. By using a lifecycle approach, this book discusses the latest technology, compliance developments, and regulatory considerations and trends, from process design, to divesting. As part of the Expertise in Pharmaceutical Process Technology series edited by Michael Levin, this book incorporates numerous case studies and real-world examples that address timely problems and offer solutions to the daily challenges facing practitioners in this area.

Drug Delivery Systems

• 1st Edition
• October 22, 2019
• Rakesh Kumar Tekade
• English
• Hardback 978-0-12-814487-9

  9 7 8 - 0 - 1 2 - 8 1 4 4 8 7 - 9
• eBook 978-0-12-814508-1

  9 7 8 - 0 - 1 2 - 8 1 4 5 0 8 - 1

Drug Delivery Systems examines the current state of the field within pharmaceutical science and concisely explains the history of drug delivery systems, including key developments. The book translates the physicochemical properties of drugs into drug delivery systems administered via various routes, such as oral, parenteral, transdermal and inhalational. Regulatory and product development topics are also explored. Written by experts in the field, this volume in the Advances in Pharmaceutical Product Development and Research series deepens our understanding of drug delivery systems within the pharmaceutical sciences industry and research, as well as in chemical engineering. Each chapter delves into a particular aspect of this fundamental field to cover the principles, methodologies and technologies employed by pharmaceutical scientists. This book provides a comprehensive examination that is suitable for researchers and advanced students working in pharmaceuticals, cosmetics, biotechnologies, and related industries.

Mosby’s Pharmacy Technician Exam Review

• 4th Edition
• June 29, 2019
• James J. Mizner
• English
• Paperback 978-0-323-49724-4

  9 7 8 - 0 - 3 2 3 - 4 9 7 2 4 - 4
• eBook 978-0-323-56940-8

  9 7 8 - 0 - 3 2 3 - 5 6 9 4 0 - 8

Prepare for success on your certification exam! Mosby's Pharmacy Technician Exam Review, 4th Edition provides a complete review of core knowledge, thousands of review questions, and nine practice exams – plus a custom online engine that allows for unlimited opportunities to practice specific topics or create unique simulated exams. A bulleted, outline format makes review easier, reinforcing understanding with full-color illustrations, photographs, and summary tables. All questions reflect the latest exam blueprints. This resource provides you comprehensive support every step of the way for entry-level or sterile compounding certification.

Equipment Qualification in the Pharmaceutical Industry

• 1st Edition
• June 13, 2019
• Steven Ostrove
• English
• Paperback 978-0-12-817568-2

  9 7 8 - 0 - 1 2 - 8 1 7 5 6 8 - 2
• eBook 978-0-12-817569-9

  9 7 8 - 0 - 1 2 - 8 1 7 5 6 9 - 9

Equipment Qualification in the Pharmaceutical Industry provides guidance and basic information for the preparation of a quality qualification program. It has been noted that there is a general lack of understanding in the industry, especially for those new to the industry, as to what constitutes a compliant qualification program. Even experienced professionals have felt a lack of security in reaching a compliant state. This book outlines a guideline for the preparation and execution of qualification protocols including the installation (IQ), operational (OQ), and performance (PQ) protocols. It discusses the importance of related qualification programs (e.g., quality systems, commissioning, computer system, and cleaning) and how to incorporate them into a fully compliant qualification program. Furthermore, it provides matrices of what could be included in each type of protocol for major types of process equipment. While primarily for people entering the pharmaceutical industry, those established in the field will benefit from the multiple examples and matrices as well as integration of related systems. Equipment Qualification in the Pharmaceutical Industry provides students and pharmaceutical scientists a guideline for the preparation and execution of qualification (installation, operational, and performance) protocols.

The Core Model

• 1st Edition
• June 4, 2019
• Ibis Sanchez Serrano
• English
• Paperback 978-0-12-814293-6

  9 7 8 - 0 - 1 2 - 8 1 4 2 9 3 - 6
• eBook 978-0-12-814294-3

  9 7 8 - 0 - 1 2 - 8 1 4 2 9 4 - 3

The Core Model: A Collaborative Paradigm for the Pharmaceutical Industry and Global Health Care develops the innovative core model, an organizational research and design paradigm and economic theory that proposes a collaborative approach to resolving global health issues and improving the productivity of drug development. The model proposes that scientific collaboration does not occur in an unstructured manner, but actually takes place within a highly structured order where knowledge is transferred, integrated and finally translated into commercial products. An understanding of this model will help solve the global pharmaceutical industry´s productivity problems and address important global health care and economic issues. This book is useful to researchers, advanced students, regulators, and management in pharmaceutical industries, as well as healthcare professionals, those working in health economics, and those interested in scientific innovation processes.

Biomaterials and Bionanotechnology

• 1st Edition
• May 29, 2019
• Rakesh Kumar Tekade
• English
• Hardback 978-0-12-814427-5

  9 7 8 - 0 - 1 2 - 8 1 4 4 2 7 - 5
• eBook 978-0-12-814428-2

  9 7 8 - 0 - 1 2 - 8 1 4 4 2 8 - 2

Biomaterials and Bionanotechnology examines the current state of the field within pharmaceutical sciences and concisely explains the history of biomaterials including key developments. Written by experts in the field, this volume within the Advances in Pharmaceutical Product Development and Research series deepens understanding of biomaterials and bionanotechnology within drug discovery and drug development. Each chapter delves into a particular aspect of this fast-moving field to cover the fundamental principles, advanced methodologies and technologies employed by pharmaceutical scientists, researchers and pharmaceutical industries to transform a drug candidate or new chemical entity into a final administrable dosage form, with particular focus on biomaterials and bionanomaterials. This book provides a comprehensive examination suitable for researchers working in the pharmaceutical, cosmetics, biotechnology, food and related industries as well as advanced students in these fields.

Pharmaceutical Care in Digital Revolution

• 1st Edition
• March 15, 2019
• Claudia Rijcken + 1 more
• English
• Paperback 978-0-12-817638-2

  9 7 8 - 0 - 1 2 - 8 1 7 6 3 8 - 2
• eBook 978-0-12-817639-9

  9 7 8 - 0 - 1 2 - 8 1 7 6 3 9 - 9

Pharmaceutical Care in Digital Revolution demonstrates how blending human and digital pharmaceutical care can establish optimal Apothecary Intelligence (AI). Organized into four parts, it examines digital health advances that will synergize the pharmaceutical care process and prepares stakeholders for a dynamic future, fueled with innovation. Beginning with the global picture on health care systems, patients’ expectations, and current pharmaceutical care practices, the book covers details of relevant digital technologies as well as compliance, ethical, educational, and cultural aspects to take successful steps towards digital pharmaceutical care. The text includes links to lectures and technology facts, tutorials on how to implement advances in your own working environment, and examples of stakeholders who are successful in building synergy between digital and pharma. Pharmaceutical Care in Digital Revolution is a practical resource to equip pharmaceutical care stakeholders, such as pharmacists, physicians, pharmacy technicians, and students as well as those in surrounding ecosystems like payers or regulators. It is a crucial reference to understand how technological innovation is changing the paradigm in which we provide current and future pharmaceutical care and how to keep it accessible, affordable, and sustainable.