1000885 Speaker Data Sheet, Why should you attend/Description of the topic
3000025 Software Validation Utilizing Principles of Lean Documents and Lean Configuration
Also second part of:
Why should you attend/Description of the topic
You will soon be overwhelmed by continuing to apply paper document methods and approaches to software configuration and validation.
Rather than wait to be surprised by unexpected situations, or to implement requirements haphazardly, it is better to understand what the hands-on challenges of dynamic requirements as they push the boundaries of technology and new applications.
If you are already 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, and now realize a different way is needed, this webinar is something that will give you a different perspective and a very different approach that you can use.
This webinar is an overview of the coming changes and their implications, using a new approach yet is based upon solid principles and proven practices.
All life science businesses are required to maintain their Quality Management System (QMS) processes in a state of control, via controlled documents and objective evidence in the form of records.
New approaches to software validation will help avoid many of the structural costs with a major endeavor by removing legacy methods that applied to paper systems. This will also set the stage for further integration with other software systems and modules.