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1
The medical device engineers' handbook
Middletown, Delaware : ValidationResources.org, 2017Format: Book
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2
A practical field guide for ISO 13485:2003
Milwaukee, Wisconsin : ASQ Quality Press, 2012Format: Electronic eBookFull text (Emerson users only)
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3
Cost-contained regulatory compliance : for the pharmaceutical, biologics, and medical device industries
Hoboken, N.J. : John Wiley & Sons, 2011Format: Electronic eBookFull text (Emerson users only)
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Full text (Wentworth users only)
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4
Cleaning and Cleaning Validation : A Biotechnology Perspective
London : Taylor and Francis, 2017
First edition.Format: Electronic eBookFull text (WIT users only)
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5
Medical devices : managing the mismatch : an outcome of the Priority Medical Devices project
Geneva : World Health Organization, 2010Format: Electronic eBookFull text (Emerson users only)
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6
Fundamentals of US regulatory affairs.
Rockville, MD : Regulatory Affairs Professionals Society, 2007
5th ed.Format: Book
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7
Validation standard operating procedures a step-by-step guide for achieving compliance in the pharmaceutical, medical device, and biotech industries
New York : Taylor & Francis, 2006
2nd ed.Format: Electronic eBookFull text (WIT users only)
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8
Validation standard operating procedures a step-by-step guide for achieving compliance in the pharmaceutical, medical device, and biotech industry
Boca Raton [Fla.] : St. Lucie Press, 2002Format: Electronic eBookFull text (WIT users only)
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9
Risk management for medical device manufacturers
Milwaukee, Wisconson : Quality Press, 2022Format: Electronic eBookFull text (Wentworth users only)
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10
Fundamentals of US regulatory affairs
Rockville, MD : Regulatory Affairs Professionals Society, 2013
8th ed.Format: Book
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11
Design controls for the medical device industry
Boca Raton : Taylor & Francis, 2003Format: Electronic eBookFull text (Wentworth users only)
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12
Business plans handbook. Volume 6 : a compilation of actual business plans developed by small businesses throughout North America
Detroit, Mich. : Gale, 1999Format: Electronic eBookAccess E-Book
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13
Software development and quality assurance for the healthcare manufacturing industries
Englewood, Colo. : Interpharm Press, 2002
3rd ed.Format: Electronic eBookFull text (WIT users only)
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14
The Impact of academic research on industrial performance
Washington, D.C. : National Academies Press, 2003Format: Electronic eBookFull text (Emerson users only)
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15
Medical device regulation in the United States : a historical and evolutionary review
Format: Thesis Book
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16
Cost-contained regulatory compliance for the pharmaceutical, biologics, and medical device industries
Hoboken, N.J. : John Wiley & Sons, 2011Format: Electronic eBookAccess E-Book
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17
Post approval clinical studies for high risk Chinese medical devices : Global Harmonization Task Force to the rescue
Format: Thesis Book
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18
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19
SMEs and European integration internationalisation strategies
London ; New York : Routledge, 2002Format: Electronic eBookAccess E-Book
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20
The FDA and worldwide quality system requirements guidebook for medical devices
Milwaukee, Wis. : ASQ Quality Press, 2008
2nd ed.Format: Electronic eBookFull text (Emerson users only)
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