Regulation of medicines & medical devices
Regulation of medicines & medical devices
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Microneedles: The Future of Drug Delivery
£136.70This book equips readers with a comprehensive understanding of microneedles; from percutaneous absorption to microneedles production, characterization, applications in drug delivery and diagnosis, to practical perspectives on the development, manufacturing, regulatory issues, and commercialization of microneedles. Learn MorePublication date 04 July 2023
By Taylor & Francis Ltd -
Tunneling Field Effect Transistors: Design, Modeling and Applications
£113.15This book will give insight into emerging semiconductor devices from their applications in electronic circuits, which are the backbone of electronic equipment. It provides desired exposure to the ever-growing field of low-power electronic devices and their applications in nanoscale devices, memory design, and biosensing applications. Learn MorePublication date 09 June 2023
By Taylor & Francis Ltd -
Tunneling Field Effect Transistors: Design, Modeling and Applications
£113.15This book will give insight into emerging semiconductor devices from their applications in electronic circuits, which are the backbone of electronic equipment. It provides desired exposure to the ever-growing field of low-power electronic devices and their applications in nanoscale devices, memory design, and biosensing applications. Learn MorePublication date 01 June 2023
By Taylor & Francis Ltd -
Emerging Drug Delivery and Biomedical Engineering Technologies: Transforming Therapy
£103.70This book highlights the advances in drug discovery and delivery and the need for emerging technologies. The text describes new micro and nanofabrication techniques, including methods like electrohydrodynamic processes, additive manufacturing, and microfluidics, which have potential to produce drug delivery systems that were not possible before. Learn MorePublication date 30 March 2023
By Taylor & Francis Ltd -
The Law and Regulation of Medicines and Medical Devices
£141.45A practical guide for legal, medical, and pharmaceutical professionals, offering an authoritative and comprehensive source of expertise on the legislation and case law governing regulation of medicines and medical devices, and their liability under consumer protection law in the UK and EU. Learn MorePublication date 04 October 2021
By Oxford University Press -
Nanoaerosols, Air Filtering and Respiratory Protection: Science and Practice
£94.25Respiratory protective devices (RPD) serve to protect against air pollution in the work environment and in everyday life. This book provides the essential lifesaving knowledge for choosing the proper RPD against the nanoparticles. Ideal for the safety engineer and the health and safety professionals in the field. Learn MorePublication date 03 August 2020
By Taylor & Francis Ltd -
Excellence Beyond Compliance: Establishing a Medical Device Quality System
£36.75Publication date 24 May 2018
By Taylor & Francis Ltd -
ISO 13485:2016: A Complete Guide to Quality Management in the Medical Device Industry, Second Edition
£108.40Publication date 14 May 2018
By Taylor & Francis Ltd -
Big Data in Medical Image Processing
£169.70The book provides an automated system that could retrieve images based on user's interest to a point of providing decision support. It will help medical analysts to take informed decisions before planning treatment and surgery. It will also be useful to researchers who are working in problems involved in medical imaging. Learn MorePublication date 31 January 2018
By Taylor & Francis Ltd -
Regulatory and Pharmacological Basis of Ayurvedic Formulations
£141.45Publication date 14 June 2016
By Taylor & Francis Inc -
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Mobile Point-of-Care Monitors and Diagnostic Device Design
£60.30Publication date 25 August 2014
By Taylor & Francis Inc -
FDA Regulatory Affairs: Third Edition
£141.45Examines harmonization of US Federal Food, and Cosmetic Act with international regulations as they apply to human drug and device development, research, and marketing. Focusing on drug approval process, cGMPs, GCPs, quality system compliance, and documentation requirements, this title is suitable for those involved in pharmaceutical regulation. Learn MorePublication date 28 February 2014
By Taylor & Francis Ltd
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