Open Daily: 10am - 10pm | Alley door pickup 10am - 7pm 3038 Hennepin Ave Minneapolis, MN
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  • Open Daily: 10am - 10pm
    Alley-side Pickup: 10am - 7pm

    3038 Hennepin Ave Minneapolis, MN
    612-822-4611

Open Daily: 10am - 10pm | Alley-side Pickup: 10am - 7pm
3038 Hennepin Ave Minneapolis, MN
612-822-4611
ISO 13485 for Engineers

ISO 13485 for Engineers

Browne, Priscilla

Paperback

Medical ReferenceTechnology & Engineering

ISBN13: 9798778002975
Publisher: Independently Published
Published: Dec 1 2021
Pages: 108
Weight: 0.25
Height: 0.22 Width: 5.00 Depth: 8.00
Language: English
This book is written to provide Quality engineers, medical engineers, device engineers with a practical and insightful companion to understand ISO 13485, Quality Management system for medical devices. It provides a straight-to-the-point perspective which should assist in the interpretation of the standard and provide a benchmark for what is expected in the application of the standard and compliance for industry. ISO 13485:2016 is an international standard for the quality management of medical devices. It is of value and applicable to a number of business areas that are involved in the various stages of a medical device and its product lifecycle. It may be applied by a design company, manufacturer, raw material supplier, calibration service, sterilization services or distributer. The scope of the standard covers:
  • design and development
  • production, storage and distribution
  • installation
  • servicing (if required)
  • decommissioning and disposal
In particular, manufacturers of medical devices and typically mandated by regulatory bodies to comply with ISO 13484, and must demonstrate compliance and application of the standard subject to certification and an audit process. FDA, 21 CFR Part 820 is another example of a Quality Management system. While its official designation is a Quality System (QS) it serves a similar purpose to ISO 13485- Quality management system for medical devices. However, there is an important distinction. 21 CFR Part 820 has a regulatory standing in the United states. While many competent authorities require the application of ISO 13485, the framework of ISO 13485 is a standard opposed to a regulation.

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