The 6 Most Common Problems in FDA Software Validation and Verification
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Deadline: October 17, 2020 | Date: October 27, 2020
Venue/Country: U.S.A
Updated: 2020-09-29 16:05:44 (GMT+9)
Call For Papers - CFP
This webinar describes the validation planning process with particular emphasis on avoiding six common pitfalls. Increased use of software from automated manufacturing and quality systems means increased exposure. Most recalls can be traced back to computerized equipment, exposing the validation process to scrutiny. Corporate uncertainty leads to inaction and “wheel spinning.” Many companies struggle with understanding how to avoid major mistakes when validating software to FDA standards.Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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