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The Medical Device R&D Handbook | Effective FMEAs | Quality Risk Management in the FDA-Regulated Industry | Handbook of Human Factors in Medical Device Design | Medical Device Design
The second edition of a bestseller, Design Controls for the Medical Device Industry provides a comprehensive review of the latest design control requirements, as well as proven tools and techniques to ensure your companyâs design control program evolves in accordance with current industry practice. The text assists in the development of an effective design control program that not only satisfies the US FDA Quality System Regulation (QSR) and ISO 9001 and 13485 standards, but also meets todayâs third-party auditor/investigator expectations and saves you valuable time and money.
The authorâs continual participation in FDA QSR inspections and Notified Body ISO audits is reflected in updates to all chapters and appendices of the book, now bursting at the seams with:
- New coverage of ISO 9001 and 13485 design control requirements
- More real-world examples from the medical device industry
- Additional detail for greater understanding and clarity
- Fresh templates for practical implementation
- Extensive references for further study
The book addresses design control elements such as design planning, input, output, review, verification, validation, change, transfer, and history, as well as risk management inclusive of human factors and usability, biocompatibility, the FDA Quality System Inspection Technique (QSIT) for design controls, and medical device regulations and classes in the US, Canada, and Europe.
About: The second edition of a bestseller, Design Controls for the Medical Device Industry provides a comprehensive review of the latest design control requirements, as well as proven tools and techniques to ensure your companyâs design control program evolves in accordance with current industry practice.
About: 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.
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