Overview
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Move forward with greater confidence
Considering a transition from Analyst software to SCIEX OS software, but concerned about validation?
Join this webinar to learn how computerized system validation can help protect data integrity and support compliance throughout the transition. See how laboratory requirements can be translated into configured, tested and documented controls, and discover the practices that can help maintain a validated state after implementation.
What you will learn
- Understand key data integrity principles, including the ALCOA + CCEA framework.
- Learn how computerized system validation provides objective evidence that a system has been configured, tested and documented against laboratory requirements.
- Explore compliance capabilities in SCIEX OS software, including electronic audit trails, electronic signatures, security configurations and centralized administration.
- Understand how change control, revalidation and periodic requalification help maintain a validated state.
Speakers
Meet the speaker
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Patrick Quinn-Paquet, Senior Lead Compliance Specialist at SCIEX, brings extensive experience in software security, audit trails and compliance services. He has validated at least 100 workstations for customers worldwide and has worked with regulatory agencies on the security and audit capabilities of SCIEX software.