From Drug Discovery to Production QC
Mastering Bioassays with PLA 3.0 and Tecan Spark® Multimode Reader
Course objective
Learn how to achieve GxP compliance and precision in bioassays with Stegmann Systems' PLA 3.0 software and Tecan's Spark® Multimode Reader.
Discover how you can benefit from the integrated PLA 3.0 software and Tecan's Spark® Multimode Reader in your bioassay workflows, from early drug discovery to rigorous production quality control (QC) phases. This course provides hands-on details for utilizing these powerful tools to ensure compliance, precision, and efficiency in GMP/GLP regulated environments.
Discover how PLA 3.0 and Spark can revolutionize your lab!
Spark® is for research use only. Not for use in diagnostic procedures.
Date
December 12, 2024
Time
8 am PST, 11 am EST,
4 pm GMT, 5 pm CET
DURATION
45 mins
Course TYPE
Live
What's included?
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Enhanced data accuracy and reliability
Gain proficiency in using PLA 3.0's advanced statistical tools, designed specifically for bioassay analysis, paired with the Spark® Multimode Reader's reproducible measurements across multiple detection modes. -
Regulatory compliance and qualification
Understand how to implement PLA 3.0 and SparkControl™ Magellan™ Tracker for 21 CFR Part 11-compliant workflows, with guidance on IQ/OQ procedures for the Spark® Multimode Reader. -
Streamlined workflow integration
Learn how to integrate Spark® and PLA 3.0 seamlessly for efficient data transfer, automation, and error reduction, boosting laboratory throughput and minimizing manual steps. -
Advanced data analysis and visualization
Explore PLA 3.0's capabilities for dose-response analysis, equivalence testing, and complex matrix approaches to bioassay data, critical for ATMP development and QC. -
Comprehensive support for GxP compliance
Utilize the tools and resources necessary for FDA and GAMP® 5 compliance, with access to on-demand training modules and qualification resources.
Frequently asked questions
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Who should attend?
This course is ideal for laboratory professionals in the biopharmaceutical industry, including scientists, QC analysts, and lab managers seeking to enhance their bioassay workflows and ensure regulatory compliance. -
How long is the course going to take?
The presentation takes 45 minutes. -
Where does the course take place?
Virtually through this platform. -
Is there a participant limit?
No.
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