A scientist monitors real-time bioprocess data on a screen, collected by a Raman probe inserted into a stainless steel bioreactor, illustrating the application of Raman spectroscopy for pharmaceutical manufacturing.

raman-spectroscopy-for-pharmaceutical-manufacturing

Smaller instruments, stronger data analytics, and rising regulatory acceptance position Raman spectroscopy as a critical tool for real-time insight in modern pharma and biopharma manufacturing.

Raman Spectroscopy Gains Ground in PAT and Pharma 4.0

Articles

A modern brewing facility with large stainless steel fermentation tanks on the production floor and a glass-enclosed on-site laboratory on the right where a technician performs analytical tests for brewing quality control.

brewing-quality-control-and-separation-science

Modern analytical tools are reshaping brewing quality control and giving labs deeper insight into ingredients, contaminants, and flavor drivers.

Expert Q&amp;A: Advanced Analytical Science for Brewing Quality Control

Lab technician pouring water sample into beaker for EPA Method 1633 PFAS testing analysis

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Merck banner reading “PFAS in Water: See the App Note” with a green “Download Now” button on a white background.

Separation Science

Merck

Testing for parts-per-trillion levels of PFAS in water requires labs to manage contamination, stabilize extraction conditions, and limit chromatographic drift.

EPA Method 1633: Three Control Points That Keep PFAS Quantitation Stable

A gloved hand holds a dual-layer solid-phase extraction cartridge against a river background, illustrating the advanced technology used for environmental SVOC analysis.

solid-phase-extraction-for-svoc-analysis

Method 8270E and solid-phase extraction are transforming semi-volatile organic compound (SVOC) testing with higher recoveries, faster throughput, and greener chemistry.

Rewriting the Rules of SVOC Extraction: How Solid-Phase Innovation Is Advancing Environmental Analysis

Holly Lee explains how labs strengthen PFAS and mycotoxin analysis through smarter chromatography, cleanup, and high-resolution mass spectrometry.

Strengthening Food Testing Workflows for PFAS and Mycotoxins

A stylized DNA helix transitioning from glowing blue nodes containing pharmaceutical icons to glowing green nodes containing sustainability icons against a digital background. This visualizes the pharmaceutical industry's shift towards sustainable lab operations and the reduction of Scope 3 emissions through My Green Lab's Converge Initiative.

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The Converge Supplier Initiative brings pharma and biotech together with suppliers to improve lab sustainability and align with global climate goals.

Driving Sustainable Change Across the Pharmaceutical Supply Chain with My Green Lab&#39;s Converge Initiative&nbsp;

A dynamic 3D array of blue and orange ball-and-stick molecular structures, illustrating the complex mixtures analyzed in chiral CE separations.

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How analytical chemists are leveraging CE and QbD to meet strict regulatory standards for chiral drugs and impurity limits.

Mastering Chiral Separations and Impurity Profiling with Capillary Electrophoresis

A scientist in a laboratory analyzes a PCA Score Plot on a computer screen, illustrating the use of chemometrics in biotech and pharma for data interpretation.

chemometrics-in-biotech-and-pharma

This guide shows analytical scientists how to use chemometrics to optimize workflows, strengthen decisions, and support quality manufacturing.

Chemometrics in Biotech &amp; Pharma: An Analytical Scientist&rsquo;s Guide

Two unlabeled injection pens resting on a stainless steel laboratory bench, representing the finished product samples that undergo rigorous GLP-1 peptide impurity profiling.

glp-1-peptide-impurity-profiling

Achieve accurate results in GLP-1 peptide impurity profiling by mastering the separation of D-isomers and oxidation variants.

GLP-1 Peptide Impurity Profiling: Separating D-Isomers, Oxidation States, and Truncations

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Illustration comparing NTA size distribution and flow cytometry scatter detection used in exosome quantification.

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This guide compares NTA and flow cytometry with respect to calibration, detection limits, reproducibility, and regulatory compliance.

Accurate Exosome Quantification: NTA vs Flow Cytometry

Conceptual image of green plant symbolizing EPA proposed revisions

epa-proposed-revisions

EPA proposed revisions aim to reduce the burden of PFAS reporting requirements for manufacturers and importers.

Understanding the EPA&rsquo;s Proposed PFAS Reporting Revisions

A top-down view of various size exclusion chromatography (SEC) columns with colored caps, illustrating diverse options for SEC column selection guide.

sec-selection-guide

Optimizing resolution and lifetime with the right SEC column choice

Articles

Raman Spectroscopy Gains Ground in PAT and Pharma 4.0

Expert Q&A: Advanced Analytical Science for Brewing Quality Control

EPA Method 1633: Three Control Points That Keep PFAS Quantitation Stable

Rewriting the Rules of SVOC Extraction: How Solid-Phase Innovation Is Advancing Environmental Analysis

Strengthening Food Testing Workflows for PFAS and Mycotoxins

Driving Sustainable Change Across the Pharmaceutical Supply Chain with My Green Lab's Converge Initiative

Mastering Chiral Separations and Impurity Profiling with Capillary Electrophoresis

Chemometrics in Biotech & Pharma: An Analytical Scientist’s Guide

GLP-1 Peptide Impurity Profiling: Separating D-Isomers, Oxidation States, and Truncations

Accurate Exosome Quantification: NTA vs Flow Cytometry

Understanding the EPA’s Proposed PFAS Reporting Revisions

The Essential SEC Column Selection Guide: Practical Chemistry for Biopharma Analysts