Compliance4All, Online
2017-03-14
Overview: In this webinar, we apply the Theory of Lean documents and its corollary
Theory of Lean Configuration to present a fresh approach to following 21
CFR Part 820.
Why Should you attend: If you are constantly struggling to create, manage, and maintain all of
the information found in controlled documents, all of which are often
redundant, repetitive, and clustered together in an awkward manner, this
webinar is something that will give you a different perspective and a very
different approach that you can use.
Areas Covered in the Session: Brief introduction to Lean Documents and Lean Configuration Quality System Regulation, 21 CFR Part 820, and ISO 13485 as these
apply to design control documents Basic functions found in a life sciences manufacturing plant Key types of controlled documents and records for manufacturing Quality Management System (QMS) elements controlled via
documentation Bringing it all together
Who Will Benefit: Managers, Supervisors, Directors, and Vice-Presidents R&D Manufacturing Engineering Design Assurance Quality Assurance Operations Document Control
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