Regulation of medicines & medical devices
Regulation of medicines & medical devices
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Biomaterials and Materials for Medicine: Innovations in Research, Devices, and Applications
£132.00Publication date 09 September 2021
By Taylor & Francis Ltd -
Deep Learning for Biomedical Applications
£113.15Publication date 01 July 2021
By Taylor & Francis Ltd -
Excellence Beyond Compliance: Establishing a Medical Device Quality System
£37.70Publication 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 -
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Drug and Device Product Liability Litigation Strategy
£207.45Each year sees thousands of lawsuits filed to seek recovery from manufacturers of pharmaceuticals and medical devices. In this high-stakes, rapidly-evolving field of practice, this book provides valuable assistance to lawyers through strategic guidance, practice pointers, and discussion on key shifts in the legal landscape since the first edition. Learn MorePublication date 18 January 2018
By Oxford University Press -
Regulatory and Pharmacological Basis of Ayurvedic Formulations
£141.45Publication date 16 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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