Quality control is a vital step in the pharmaceutical industry; it includes the testing of raw materials, product intermediates and final drug products, to ensure they meet the specifications related to their safety, stability, and efficacy.
Typical quality control processes that we support with our high-end laboratory balances include sample preparation and management.
See how we can address your weighing challenges in your QC process.
Modern HPLC Strategies That Improve Retention and Peak Shape for Basic Analytes
August 16th 2024In high-performance liquid chromatography (HPLC), it is common for bases and unreacted ionized silanols on silica-based columns to cause irreproducible retention, broad peaks, and peak tailing when working with basic analytes. David S. Bell, Lead Consultant at ASKkPrime LLC offers innovative HPLC strategies that can help mitigate such issues.
Advancing Chromatographic Analysis: A Novel Composite Technology for SPE
July 22nd 2024Solid Phase Extraction (SPE) is vital for chromatographic analysis. However, traditional loose-packed SPE products struggle with channelling and inconsistent resin mass, resulting in poor recovery and reproducibility. Discover how innovative composite technology overcomes these challenges to transform sample preparation, ensuring reliable and sensitive chromatographic data.
Unveil the Power of Raman Spectroscopy for Real-Time Product Insight
May 20th 2024Raman spectroscopy is the ideal approach to compositional analysis and provides great versatility. In this Q&A, Tom Dearing, Senior Staff Scientist, and John Richmond, Senior Sales Manager, both at Thermo Fisher Scientific, provide an overview of the MarqMetrix All-In-One Process Raman Analyzer.