The 6 Most Common Problems in FDA Software Validation and Verification 2015
12 Feb 2015
Webinar
Key Topics
Review of FDA software validation requirements
Outline of FDA regulations as applied to software
The 6 Most Common Problems in FDA Software Validation & Verification
Why validation makes good business sense
Advice on successful validation project staffing
Strategies on how to avoid the most common problems
Who should Attend
Attendees from FDA regulated Medical Device, Pharmaceutical, Diagnostics, Biotech and Biological manufacturers, including:
QA / QC managers, executives and personnel
System owners - responsible for keeping individual systems in validation
Validation specialists
IT / IS managers and personnel
Consultants
Software quality reviewers
Past Events
The 6 Most Common Problems in FDA Software Validation and Verification 2015 - 12 Feb 2015, Webinar (10571)
The 6 Most Common Problems in FDA Software Validation and Verification 2026
Important
Please, check "The 6 Most Common Problems in FDA Software Validation and Verification" official website for possible changes, before making any traveling arrangements
