Unlock High-Fidelity Pharma Testing with Raman Spectroscopy

Pharmaceutical quality control is under constant pressure with tighter regulatory oversight, complex supply chains, shrinking release timelines, and the growing need for real-time assurance. Raman spectroscopy has rapidly emerged as one of the most powerful analytical tools to meet these demands, delivering molecular-level insights with speed, precision, and minimal sample preparation.

This Before You Buy eBook—featuring insights from Sudhir Dahal, Product Manager for Raman Spectroscopy at Thermo Fisher Scientific—provides a technically rigorous guide to implementing and optimizing Raman spectroscopy across the pharmaceutical testing continuum.

What’s Inside the eBook

• A step-by-step breakdown of Raman spectroscopy fundamentals
• How Raman fits within pharmaceutical QC, regulatory frameworks, and ICH guidelines
• Case-relevant examples of polymorph detection, stress mapping, and blend uniformity analysis
• Practical considerations for method validation, workflow integration, and data management
• Future-focused insights into automation, AI-driven spectral analysis, and portable Raman deployment
• A full technical profile of the Thermo Scientific DXR3 SmartRaman spectrometer

Who Should Read This eBook?

• Pharmaceutical QC/QA managers
• Analytical development scientists
• Formulation and solid-state chemists
• Manufacturing and PAT engineers
• Laboratory directors evaluating technology upgrades
• Materials scientists working in pharma and biopharma

Download the eBook and see how Raman can strengthen your materials testing framework and accelerate your move toward faster, more robust QC operations.