Safe and Sound Software: Creating an Efficient and Effective Quality System for Software Medical Device Organizations (e-Book)
Faris, Thomas H.
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This book provides information and recommendations to help regulatory affairs and quality managers and consultants of software medical device design and development organizations navigate the complex course of regulatory compliance, operational excellence, product quality, and customer satisfaction to create an effective and efficient quality system. Software organization executives, functional managers, and other interested coworkers can also utilize this book to secure a general understanding of the subject matter.Many consulting firms, industry associations, and educational institutions present regulatory and quality training opportunities to regulatory and quality students and professionals. However, most training events focus on specific topics or requirements, such as ISO 9000, FDA Quality System Regulations, Six Sigma, vendor qualification, and software design control. Regulations and standards typically provide concise statements of requirements, but not much more. This book fills that gap in information available to regulatory and quality professionals in the software medical device industry. The resultant operational management system outlined in Part II, the Software Medical Device Quality System Guidelines, provides these professionals with recommendations and considerations for implementing the potentially duplicative requirements in a manner that reduces the bureaucracy of the system and adds value toward satisfying the organization’s objectives. Part II is also included on a CD-ROM accompanying the book.
368 pages.
ISBN 978-0-87389-674-0.
Adobe Acrobat PDF file.
2006
Item: E1262
Member Price: $33.00
List/Forum-Division Price: $55.00
Related Products:
Safe and Sound Software: Creating an Efficient and Effective Quality System for Software Medical Device Organizations
Faris, Thomas H.
Requests for multiple subscriptions should be directed to ASQ Customer Care at 800-248-1946 or 414-272-8575.
About the Author(s):
Thomas H. Faris is currently the Vice President of RA/QA and chief privacy officer at IMPAC Medical Systems, Inc., a developer of healthcare information systems designed specifically for the radiation and medical oncology fields. Faris is an experienced quality champion of successful efforts to implement quality management systems that satisfy the FDA's Quality System Regulations and achieve certification to ISO 9001, the Medical Device Directive, and all other related standards. He has a BS degree in justice studies from Arizona State University, an MS in quality assurance from California State University Dominguez Hills, and a doctorate of jurisprudence from Golden Gate University School of Law. Faris is a state bar certified attorney in the state of California. He is an ASQ Senior member, Certified Quality Manager, and Certified Quality Auditor.
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