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FDA Quality System Regulation for Medical Devices 21 CFR Part 820: A Practitioners Guide to Management Controls sections 820.20 Management ... 820.22 Quality Audit, and 820.25 Personnel Paperback December 19, 2015
Donald G. Daugherty is an accomplished medical device quality assurance professional with over 25 years of experience.
FDA Quality System Regulation for Medical Devices 21 CFR Part 820: A Practitioners Guide to Management Controls sections 820.20 Management ... 820.22 Quality Audit, and 820.25 Personnel Paperback December 19, 2015
Item #: 19567369

FDA Quality System Regulation for Medical Devices 21 CFR Part 820: A Practitioners Guide to Management Controls sections 820.20 Management ... 820.22

Item #: 19567369

XCD 65

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Donald G. Daugherty is an accomplished medical device quality assurance professional with over 25 years of experience.
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What Stands Out

Comprehensive Guidance
This guide provides exhaustive insights into FDA Quality System Regulations, enabling practitioners to navigate complex management controls effectively, ensuring compliance and minimizing risk in medical device operations.
Practical Application
Designed for real-world use, this book translates regulatory requirements into actionable steps for quality audits and personnel management, streamlining processes for better regulatory adherence and organizational efficiency.
Expert Insights
Authored by industry experts, the guide imparts valuable knowledge and best practices, empowering readers to implement robust quality management systems tailored to meet stringent FDA standards.

Product Details

Find the best deals on FDA Quality System Regulation for Medical Devices on Ubuy Grenada. A comprehensive guide to management controls, quality system development, and compliance with expert insights from Donald G. Daugherty.
Publisher CreateSpace Independent Publishing Platform
Publication date December 19, 2015
Language English
Print length 58 pages
ISBN-10 1522840249
ISBN-13 978-1522840244
Item Weight 3.2 ounces (90.72 grams)
Dimensions 6 x 0.14 x 9 inches (15.2 x 0.4 x 22.9 cm)

Who Should Buy?

Suitable For
  • Quality Managers

    A comprehensive guide for quality managers implementing FDA regulations and ensuring compliance within medical device companies.

  • Regulatory Consultants

    Useful for consultants advising medical device companies on FDA regulations, facilitating easier comprehension of management controls.

  • Medical Device Companies

    Ideal reference for companies involved in medical device design and manufacturing, aiming for compliance with FDA quality standards.

Not Suitable For
  • General Public

    Not suitable for the general public, as it contains specialized technical information relevant only to professionals.

  • Academic Researchers

    Limited applicability for researchers focused on theoretical studies rather than practical implementation of FDA regulations.

  • Non-FDA Markets

    Not applicable for professionals in industries outside of FDA-regulated environments, lacking relevant content for those markets.

Product Description

FDA Quality System Regulation for Medical Devices 21 CFR Part 820: A Practitioners Guide to Management Controls sections 820.20 Management ... 820.22 Quality Audit, and 820.25 Personnel Paperback December 19, 2015

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Customer Questions & Answers

  • Question: What is Donald G. Daugherty's area of expertise?

    Answer: Donald G. Daugherty is highly knowledgeable in requirements of FDA QSR 820, ISO 13485, and ISO 14971, and manufacturing process validation.
  • Question: What are some of Donald G. Daugherty's skills?

    Answer: Donald G. Daugherty is skilled in statistical techniques, process improvement, problem solving, and root cause analysis.
  • Question: What organizations is Donald G. Daugherty affiliated with?

    Answer: Donald G. Daugherty is a senior member of the American Society for Quality (ASQ) and maintains professional certifications through ASQ as a Certified Six Sigma Black Belt, Quality Engineer, and Quality Auditor.

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