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All Events in United States (3)
May 7Tuesday
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Common Problems with Software Validation Processes - Webinar By GlobalCompliancePanel
May 7, 2013 from 10am to 11:30am – United States Overview: This webinar covers the fundamentals of 21 CFR Part 11, software validation, and computer system validation. It provides details for company compliance including GAMP, qualification, and va… Organized by GlobalCompliancePanel | Type: webinar, healthcare, medical, device, pharmaceutical, clinical
September 12Thursday
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The DHF, Technical File and Design Dossier - Similarities, Differences and The Future
September 12, 2013 at 9am to September 13, 2013 at 6pm – United States Overview: One of our most popular subjects, continuously updated with the latest U.S. FDA and European Union requirements. As U.S. companies go global, they must meet different product design documen… Organized by John Robinson | Type: conference
September 26Thursday
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2-day In-person Seminar on “Writing and Enforcing Effective SOPs” at Minneapolis
September 26, 2013 at 9am to September 27, 2013 at 6pm – United States Overview: Writing SOPs or procedural documents can be challenging at times. However, writing SOPs is overall a straightforward process. However, enforcing what you already created and implemented in… Organized by John Robinson | Type: conference
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