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Automation in the Validated Enterprise

November 29, 2018
08:30 AM to 11:45 AM EST

Automation in the validated enterprise

Automation in the Validated Enterprise

Automation has brought changes to all industries including the Life Sciences. In the area of compliance, a number of systems are available to assist the user in digitizing aspects of a given business process and deliverables, but lack built in business process intelligence to truly deliver the benefits of automation. Digitization of deliverable or “becoming paperless” must be a secondary goal when considering automation. Compliance automation systems must perform the complex checks and balances that can exist when executing and maintaining a quality process. A purpose-built systems will Increase productivity and adherence to quality by reducing human error and following enterprise standard practices, and allows employees to focus on the jobs that require critical thinking while freeing them from administrative tasks.

In this seminar we will examine the different activities and deliverable involved in Process Validation, Continued Process Verification, Computer System Validation, Equipment Qualification and Cleaning Validation. We will review these business processes and identify opportunities for automation and collaboration amongst said processes. The ultimate goal is to shed some light on what it takes to implement a practical, effective, and compliant solution that can deliver a validated enterprise.

AGENDA

8:30 AM- 9:00 AM Sign in and Coffee and snacks

9:00 AM- 11:45 AM Presentation and Discussion



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