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Risk-based CSV: Slashing Non-product Validation Costs

On-Demand Webinar | 62 minutes

Join us for this webinar to learn how to automate and centralize your CSV process into a single data repository. Seamlessly link requirements, feature based risk assessments, and corresponding assurance evidence. It is easy to use and offers dashboards and reports to help your firm easily prepare for regulatory reviews.

Non-Product Computer System Validation

Cumbersome. Laborious. Error-prone. Wasteful. Fragmented. Painful. There are many words to describe the current state of how many firms engage in over burdensome validation efforts. For those firms still approaching CSV in this manner, there is another way.

Join us for this webinar to learn how to automate and centralize your CSV process into a single data repository. Seamlessly link requirements, feature based risk assessments, and corresponding assurance evidence. It is easy to use and offers dashboards and reports to help your firm easily prepare for regulatory reviews.

In this webinar, which includes a short introductory of Non-Product Computer Systems Validation (CSV) methodology solution demonstration, expert speakers will discuss how these technologies will enable medical device companies to:

  • Enhance Your Workflow Management and enforce conformance with established processes
  • Minimize Internal & External Audit failures – rapid access to high quality evidence and findings
  • Risk Management Improvement – ensures work is contextualized

 

SPEAKERS:

Larry Sampson., Industry Specialist - Medical Devices, Siemens PLM
Javier Cubero, Systems Engineer, Medical Devices, Siemens PLM

Learn how to automate and centralize your CSV process

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