Life sciences computer system validation: An end-to-end solution is needed has been saved
Perspectives
Life sciences computer system validation: An end-to-end solution is needed
The importance of validation lifecycle management grows
It’s time for transformation. Digital validation lifecycle management solutions can shed light on the future of computer system validation.
Get the perspective: Accelerating digitization in life sciences
Why now is the time to go paperless in computer system validation
Current computer system validation (CSV) practices are becoming less effective and require a novel approach. Manual approaches are typically slow, cumbersome, and unreliable. Fragmented automation employs multiple systems across the validation lifecycle, raising the need to painfully stitch the validation assets together to form a coherent, traceable, and chronological history of validation. These disjointed and incomplete approaches to CSV can be inefficient, costly, and error-prone.
The good news? Digital validation lifecycle management solutions can shed light on the future of CSV. Discover how an end-to-end digital validation lifecycle management can help strengthen GxP compliance, enhance technology quality, and help life sciences organizations stay competitive in a changing environment.
In this perspective, you’ll learn about:
- Why a new approach to CSV is needed
- Four digital validation lifecycle management priorities that life sciences leaders should consider addressing now
- What to look for in an effective digital validation lifecycle management solution
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Satyanarayana Patloori (Pat)
Managing Director | Deloitte & Touche LLP
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