Regulation of medicines & medical devices
Regulation of medicines & medical devices
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Error-Tolerant Biochemical Sample Preparation with Microfluidic Lab-on-Chip
£84.85Publication date 25 July 2022
By Taylor & Francis Ltd -
Additive Manufacturing with Medical Applications
£113.15Publication date 21 July 2022
By Taylor & Francis Ltd -
Additive Manufacturing Processes in Biomedical Engineering: Advanced Fabrication Methods and Rapid Tooling Techniques
£103.70Publication date 18 July 2022
By Taylor & Francis Ltd -
Manufacturing of Quality Oral Drug Products: Processing and Safe Handling of Active Pharmaceutical Ingredients (API)
£65.05Publication date 07 July 2022
By Taylor & Francis Ltd -
Advanced Nanocarbon Materials: Applications for Health Care
£94.25Publication date 05 May 2022
By Taylor & Francis Ltd -
Advanced Microfluidics Based Point-of-Care Diagnostics: A Bridge Between Microfluidics and Biomedical Applications
£132.00Publication date 11 March 2022
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 -
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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