How software requirements are used in validation
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Website http://www.compliance4all.com/control/w_product/~product_id=501620LIVE?channel=ourglocal_Jan_2018_SE |
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Category Software Validation, Quality assurance, Risk analysis, Regulatory Affairs Courses Online, development of medical devices, latest software updations
Deadline: January 29, 2018 | Date: January 30, 2018
Venue/Country: Online, U.S.A
Updated: 2017-11-29 15:29:13 (GMT+9)
Call For Papers - CFP
Overview:This course is NOT a programming course. We will discuss what must be done but will not discuss methods to execute necessary testing.Why should you Attend: Testing software to prove that it works and has no bugs is not sufficient to obtain FDA approval. There are additional requirements,analyses and tests that FDA feels are necessary to prevent user injuries.Areas Covered in the Session:Software Validation more than TestingRequirements TraceabilityRisk AnalysisUnit,Integration and System TestingAlgorithm ValidationChallenges to the SoftwareConfiguration ManagementWho Will Benefit:EngineerEngineer ManagementSoftware EngineerProgrammerQuality AssuranceRegulatorySpeaker Profile:Edwin Waldbusser is a consultant retired from industry after 20 years in management of development of medical devices (5 patents). He has been consulting in the US and internationally in the areas of design control, risk analysis and software validation for the past 8 years.Event Fee: One Dial-in One Attendee Price: US$150.00Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: supportcompliance4All.com
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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