Netzealous LLC DBA - Compliance4All, Online
2019-01-29
Overview: How to develop or improve upon a Master Verification and Validation
Plan and System that meets U.S. FDA CGMP, ICH Q-series, and ISO
13485 expectations and requirements.
Why should you Attend: The billions of dollars spent by industry annually for V&V are not
providing the product safety or efficacy seemingly promised. For most
companies, the fixes are not rocket-science, but proper up-front V&V
planning and execution, documented in a corporate MVP and
implemented by other V&V documents.
Areas Covered in the Session: The 11 key documents for software validation Incorporating 21 CFR Part 11 requirements Suggested "test case" formats
Who Will Benefit: Engineering Production Operations Senior Management in Drugs
Event Fee: One Dial-in One Attendee Price: US $290.00
Contact Detail: Compliance4All DBA NetZealous, Phone: +1-800-447-9407 Email: compliance4all14@gmail.com
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