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"The United States and European Union now require the ISO 13485 Standard certification for medical device manufacturers. Written by an experienced industry professional, this practical book provides a complete guide to the ISO 13485 standard certification for medical device manufacturing in terms of quality control. It covers all the requirements of ISO 13485 and offers a step-by-step comparison between the ISO 13485 and ISO 9001, enabling a sound understanding of these new procedures"--Provided by publisher.
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Subjects
Medical instruments and apparatus, Medical instruments and apparatus industry, Equipment Design, Manufactured Materials, Handbooks, manuals, Standards, Equipment and Supplies, Quality control, Quality control, standards, Manufacturing processes, Qualité, Guides, manuels, Contrôle, Médecine, Appareils et instruments, Industrie, Normes, BUSINESS & ECONOMICS, Industries, General, BUSINESS & ECONOMICS / Industries / General, MEDICAL, Instruments & SuppliesEdition | Availability |
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ISO 13485: A Complete Guide to Quality Management in the Medical Device Industry
2017, Taylor & Francis Group
in English
1138071935 9781138071933
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3
ISO 13485: a Complete Guide to Quality Management in the Medical Device Industry
2012, Taylor & Francis Group
in English
1283350572 9781283350570
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4
ISO 13485: a complete guide to quality management in the medical device industry
2012, Taylor & Francis, CRC Press
in English
1439866112 9781439866115
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ISO 13485: A Complete Guide to Quality Management in the Medical Device Industry
2011, Taylor & Francis Group
in English
1439866120 9781439866122
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- Created August 18, 2020
- 4 revisions
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March 19, 2023 | Edited by ImportBot | import existing book |
December 12, 2022 | Edited by MARC Bot | import existing book |
December 10, 2022 | Edited by MARC Bot | import existing book |
August 18, 2020 | Created by ImportBot | Imported from Better World Books record |