Design Controls for the Medical Device Industry

Pirmais vāks
CRC Press, 2002. gada 20. sept. - 254 lappuses
This reference provides real-world examples, strategies, and templates for the implementation of effective design control programs that meet current ISO 9000 and FDA QSR standards and regulations-offering product development models for the production of safe, durable, and cost-efficient medical devices and systems.

Details procedures utilized by leading companies to successfully meet FDA and end-user requirements, manufacture high-quality products, and improve and generate profit.

Design Controls for the Medical Device Industry contains valuable guidelines that enable readers to
  • prepare for an FDA audit
  • identify consumer needs, resolve project objectives, and process inconsistencies and discrepancies
  • determine the compatibility of design specifications and manufacturing, installation, and servicing demands
  • ensure that proper design, function, and performance stipulations are understood and met
  • verify and validate design criteria and production schemes
  • eliminate confusion and prevent communication breakdowns
  • allocate and conserve resources
  • perform risk assessment analyses
  • predict potential hazards under normal and fault conditions
    Presenting blueprints for the application, evaluation, and refinement of quality assurance and performance practices-from product launch through engineering and assembly-Design Controls for the Medical Device Industry is a clear and indispensable source for biomedical, quality assurance, reliability, software, product design, manufacturing, research and development, and industrial engineers; project directors and managers; biomedical technicians; and upper-level undergraduate and graduate students in these disciplines.
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