Event
Beginning: 05/07/26
Location: Online
EzSpec‑P11 is HORIBA’s new software option for Veloci and Aqualog UV‑800 A‑TEEM systems—built to help laboratories strengthen data integrity and support FDA 21 CFR Part 11–aligned workflows. Building on the latest EzSpec platform enhancements (expanded applications, improved processing tools, and a database file system), EzSpec‑P11 adds key compliance-oriented capabilities including secure login, role-based permissions, approval records, and a comprehensive audit trail—enabled through the PLATINALINK data integrity platform.
In this session, Dr. Karen Gall will walk through how EzSpec‑P11 and PLATINALINK work together in A‑TEEM workflows—from method setup and acquisition to processing, reporting, and review. You’ll see practical examples and learn how these features can help streamline collaboration, improve traceability, and reduce risk in GMP environments where data integrity is non‑negotiable.
Who Should Attend:
1. PAT / Method Innovation Scientists driving analytical modernization and tech transfer
2. Spectroscopists and A‑TEEM Users responsible for method execution and optimization
3. R&D and Formulation Scientists needing reliable, traceable analytical workflows
4. QA/QC and Compliance Professionals supporting GMP labs and data integrity programs
What You Will Learn:
• How EzSpec‑P11 helps reinforce data integrity through secure access, permissions, and traceability
• How PLATINALINK enables audit trails, approvals, and review-ready records across A‑TEEM workflows
• Practical examples of A‑TEEM acquisition, processing, and reporting inside EzSpec‑P11
• How this solution can support Part 11–aligned practices for regulated environments (GMP and beyond)
This webinar meets 2 times. You'll be registered for all 2 sessions.
Thu, May 7, 2026 7:00 AM - 8:00 AM PDT
Thu, May 7, 2026 10:00 AM - 11:00 AM PDT
