Medical Device Software Development Management:Following FDA Guidelines for Software Validation by Parasoft CorporationWelcome, Guest      sign in | register | help


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Research Abstract
Medical Device Software Development Management:Following FDA Guidelines for Software Validation
by Parasoft Corporation

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Published on: December 31, 2012
Type of content: WHITE PAPER
Format: Unknown
Length: 10 pages
Price: FREE

Overview:

Developing software for medical devices that complies with the FDA's Quality System regulation is a
challenging endeavor that's as much a business issue as it is an engineering feat.


Read this white paper to discover:



  • Software development challenges that medical device makers face

  • Why the FDA recommends a software development lifecycle (SDLC) approach that integrates risk management strategies with principles for software validation

  • And tips for putting the FDA's recommended approach into action.

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