Regulatory ScienceMay 2025
Understanding ICH M7 and the Rise of Nitrosamine Impurity Testing
How the ICH M7 guideline has reshaped pharmaceutical impurity testing, and what it means for drug manufacturers globally.
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Isotope ChemistryApril 2025
Stable Isotope Labelling in Drug Metabolism Studies: A Practical Overview
Exploring how ¹³C, ²H, and ¹⁵N labelled compounds are used in ADME studies and bioanalytical method development.
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Synthesis ScienceMarch 2025
The Role of Reference Standards in Pharmaceutical Quality Control
Why high-purity reference standards are the cornerstone of reliable analytical testing and regulatory submissions.
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Analytical ChemistryFebruary 2025
NMR Characterisation of Impurity Reference Standards: Best Practices
A deep dive into how SRRD uses multinuclear NMR to confirm identity and purity of complex pharmaceutical impurities.
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Industry InsightJanuary 2025
N-Nitroso Compounds in Pharmaceuticals: From Risk Assessment to Reference Standards
A comprehensive look at how the pharmaceutical industry is responding to EMA and FDA guidance on nitrosamine contamination.
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Custom SynthesisDecember 2024
Complex Multi-step Synthesis: How SRRD Tackles the Most Challenging Molecules
Inside our approach to designing and executing synthetic routes for difficult, rare, or entirely novel compounds.
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