Regulation of medicines & medical devices
Regulation of medicines & medical devices
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Introduction to Flexible Electronics
£103.70Publication date 09 December 2021
By Taylor & Francis Ltd -
Functional Nanomaterials for Regenerative Tissue Medicines
£132.00Publication date 09 December 2021
By Taylor & Francis Ltd -
User Interface Requirements for Medical Devices: Driving Toward Safe, Effective, and Satisfying Products by Specification
£56.55Publication date 17 November 2021
By Taylor & Francis Ltd -
User Interface Requirements for Medical Devices: Driving Toward Safe, Effective, and Satisfying Products by Specification
£141.45Publication date 17 November 2021
By Taylor & Francis Ltd -
Bioengineering and Biomaterials in Ventricular Assist Devices
£113.15Publication date 08 October 2021
By Taylor & Francis Ltd -
Biomaterials and Materials for Medicine: Innovations in Research, Devices, and Applications
£132.00Publication date 09 September 2021
By Taylor & Francis Ltd -
Excellence Beyond Compliance: Establishing a Medical Device Quality System
£36.75Publication date 15 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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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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