The 6 Most Common Problems in FDA Software Validation & Verification - FDA Validation Webinar By ComplianceOnline
Submitted by Admin on Thu, 11/25/2010 - 09:21
12/17/2010 10:00 am
America/Chicago
This FDA Software Validation and Verification training/webinar will review the validation planning process with particular emphasis on avoiding six common pitfalls.
Areas Covered in the seminar:
- Outline of FDA regulations as applied to software.
- Review of FDA software validation requirements.
- Why validation makes good business sense.
- The 6 Most Common Problems in FDA Software Validation & Verification.
- Strategies on how to avoid the most common problems.
- Advice on successful validation project staffing.
Who will benefit:
This seminar will give valuable help to FDA regulated Pharmaceutical, Medical Device, Biotech, Diagnostics and Biological manufacturers. The staff members who will benefit include:
- System owners - responsible for keeping individual systems in validation
- QA / QC managers, executives and personnel
- IT / IS managers and personnel
- Validation specialists
- Software quality reviewers
- Consultants
Note : Use this promocode(111087) to get 10% Discount,Valid till Dec 20th.
Webinar Presenters:
ComplianceOnline Instructor - Alfonso Fuller

