Linked Data Explorerhttp://worldcat.org/entity/work/id/20546251
MDD compliance using quality management techniques
The Medical Devices Directive (MDD) is an all-encompassing document legislating for the manufacture of any medical device or material used either temporarily or permanently on or in the human body. To achieve its main objectives the MDD requires the manufacturer of all products covered by the Directive to possess a fully auditable Quality Management System consisting of Quality Policies, Quality Procedures and Work Instructions, based on the ISO 9000 standard. The book is based on the sound principles of ISO 9000 and will guide to the reader, if required, to eventually set up an ISO 9000 fully.
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http://schema.org/about
- http://id.loc.gov/authorities/subjects/sh85082949
- http://experiment.worldcat.org/entity/work/data/20546251#Topic/equipment_design_standards
- http://id.loc.gov/authorities/subjects/sh85082954
- http://id.worldcat.org/fast/1269470
- http://experiment.worldcat.org/entity/work/data/20546251#Topic/quality_control
- http://id.loc.gov/authorities/subjects/sh94006085
- http://experiment.worldcat.org/entity/work/data/20546251#Topic/medical_allied_health_services_medical_technology
- http://experiment.worldcat.org/entity/work/data/20546251#Topic/equipment_and_supplies_standards
- http://id.worldcat.org/fast/1584500
- http://id.worldcat.org/fast/1014230
- http://experiment.worldcat.org/entity/work/data/20546251#Topic/equipment_safety_standards
- http://id.worldcat.org/fast/966404
- http://experiment.worldcat.org/entity/work/data/20546251#Topic/international_cooperation
- http://id.worldcat.org/fast/1014229
- http://viaf.org/viaf/311116653
- http://id.loc.gov/authorities/subjects/sh85082952
- http://experiment.worldcat.org/entity/work/data/20546251#Topic/iso_9000_series_standards
- http://id.loc.gov/authorities/names/nr2003031903
- http://id.loc.gov/authorities/subjects/sh2011002755
http://schema.org/description
- "The Medical Devices Directive (MDD) is an all-encompassing document legislating for the manufacture of any medical device or material used either temporarily or permanently on or in the human body. To achieve its main objectives the MDD requires the manufacturer of all products covered by the Directive to possess a fully auditable Quality Management System consisting of Quality Policies, Quality Procedures and Work Instructions, based on the ISO 9000 standard. The book is based on the sound principles of ISO 9000 and will guide to the reader, if required, to eventually set up an ISO 9000 fully."@en
http://schema.org/genre
- "Electronic books"@en
http://schema.org/name
- "MDD compliance using quality management techniques"
- "MDD compliance using quality management techniques"@en