Design Controls for the Medical Device Industry - Marie B. Teixeira, Richard Bradley

Design Controls for the Medical Device Industry

Buch | Hardcover
254 Seiten
2002
Marcel Dekker Inc (Verlag)
978-0-8247-0830-6 (ISBN)
188,30 inkl. MwSt
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Contains guidelines that enable readers to prepare for an FDA audit; and, identify consumer needs, resolve project objectives, and process inconsistencies and discrepancies. This book also enables readers to determine the compatibility of design specifications and manufacturing, installation, and servicing demands.
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.

Overview; design and development planning; design input I; design input II; design outputs; design review; design verification; design validation; process validation; design transfer; design changes; the design history file; questions to expect in an audit.

Erscheint lt. Verlag 20.9.2002
Verlagsort New York
Sprache englisch
Maße 152 x 229 mm
Gewicht 499 g
Themenwelt Technik Umwelttechnik / Biotechnologie
ISBN-10 0-8247-0830-X / 082470830X
ISBN-13 978-0-8247-0830-6 / 9780824708306
Zustand Neuware
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