As biopharma organizations scale operations, expand sites, and bring assays in-house, the complexity of managing real-time PCR (qPCR) data grows alongside them. Analysis software has become a critical but often overlooked component of analytical workflows, and in regulated environments, gaps in that pipeline can quickly become costly deviations.
In this Teach Me in 10, Dr. Irene Sarkar, Scientist III in Field Applications at Thermo Fisher Scientific, introduces a real-time PCR detection software platform and explains how it automates data collection, analysis, and reporting to support GMP-compliant molecular testing. She also covers how built-in compliance features address 21 CFR Part 11 expectations and how this unified software solution scales with organizational complexity.
Watch this episode to discover:
- How automated analysis software eliminates manual interpretation steps and reduces the risk of data integrity issues
- What security, audit, and e-signature capabilities mean in practice for regulated testing environments
- Key considerations for evaluating analysis software as your analytical testing portfolio grows
