Multiparameter Measurement Systems for Pharma and Biotech

Strengthen analytical confidence with advanced physical measurement methods in Pharma and Biotech.

From buffers and excipients to complex polymers, today’s laboratories require rapid, reliable, and fully traceable data. With decades of expertise in density, refractive index, polarimetry, viscosity, and other essential physical property measurements, Anton Paar enables seamless technology transfer from R&D to QC—ensuring methods perform consistently, reproducibly, and are audit ready from day one.

In this webinar, we take a systems level look at analytical workflows across highly regulated environments. You’ll see how automated, integrated multi instrument solutions reduce operator influence, shorten turnaround time, and elevate data robustness for both routine and advanced applications. Whether you’re qualifying a coating formulation, confirming buffer composition, or verifying raw material attributes, streamlined workflows help deliver dependable, defensible results.

We’ll also highlight best in class data integrity and compliance features, including secure digital data handling, comprehensive audit trails, and full compatibility with 21 CFR Part 11. Individual sample specifications and tolerance limits can be applied automatically—generating documented, traceable pass/fail outcomes that simplify release decisions and ensure continuous audit readiness.

Join us to discover how integrated instrumentation and smart workflow design can enhance measurement confidence, reduce compliance burdens, and increase reliability from early stage development through routine QC.

Key Learning Objectives:

• Understand how physical property measurement methods—including density, refractive index, polarimetry, and viscosity—enhance analytical reliability in pharma and biotech workflows.
• Learn how to achieve seamless technology transfer from R&D to QC, ensuring methods are robust, reproducible, and audit‑ready from the start.
• Explore automated, integrated workflows minimize operator influence, reduce turnaround time, and improve data quality for routine and advanced applications.
• Gain insight into data integrity and compliance best practices, including secure digital data handling, comprehensive audit trails, and full 21 CFR Part 11 support