Electronic Validation Lifecycle Management System - Webinar

The Session will be focused on how an electronic Validation Lifecycle Management System (VLMS) can standardize and improve the efficiency of your current validation process for software, instruments, equipment, methods and processes. During the Webinar, we can demonstrate how our global regulated manufacturing clients are experiencing reduced validation cycle time and cost by 30-50%.


This session will demonstrate how an electronic Validation Lifecycle Management System will:

  • Facilitate a paperless validation process without changing the current business process
  • Standardize and improve the efficiency of your current validation process with use of templates and workflows
  • Reduce validation cycle time by 30-50%
  • Enforce consistency and enhance compliance in all types of validation process
  • Harmonize and Globalize the validation process
  • Significantly reduce the cost of validation
  • Eliminate the inefficiencies that plague manual validation process
  • Enforce validation policies and procedures that are typically buried in paper documents
  • Mitigate or avoid the commonly cited validation issues (in FDA’s warning and 483s)
  • A 21CFR Part11 compliant system that will help you organization breeze through any audit
 
Register here.

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21:26
RSS
17:25
Dates: Every Tuesday 5th Dec, 12th Dec, 19th Dec, 26th Dec