Downloadable Nitrosamine Risk Assessment Template: What Every Pharmaceutical Company Needs
Pharmaceutical companies worldwide are under increasing regulatory pressure to assess, mitigate, and report the risk of nitrosamine impurities in drug […]
Case Study: How Our Analytical Development Laboratory Accelerated a Peptide NDA Filing
In today’s competitive pharmaceutical landscape, speed and precision in regulatory filings can determine a product’s commercial success. At ResolveMass Laboratories
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Accelerating Quality Control: How GC-MS Method Development Services Support Regulatory Compliance in Canada and the United States
In the highly regulated pharmaceutical and chemical industries, regulatory compliance is not optional—it’s a legal, ethical, and scientific obligation. With
Mastering Precision: How LC-MS/MS Method Development Services Accelerate Drug Discovery in Canada and the U.S.
Liquid Chromatography with Tandem Mass Spectrometry (LC-MS/MS) has become a transformative tool in drug discovery and pharmaceutical analysis. Its precision,
How to Choose the Right Protein Quantification Lab in Montreal & Beyond
Introduction Protein quantification is a foundational analytical requirement across life sciences, from early-stage research to regulated drug development. Organizations searching
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Trace-Level PFAS Testing with LC-MS/MS: A Case Study on Consumer Product Packaging
Introduction The presence of per- and polyfluoroalkyl substances (PFAS) in consumer products has become a critical concern in public health
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Best CRO Services for Identification of an Unknown Impurity in Canada and the U.S.
Introduction: Why You Need the Right CRO for Unknown Impurity Identification In the pharmaceutical lifecycle, encountering an unexpected impurity—especially during
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How We Carried Out Identification of an Unknown Impurity in a Phase 3 API Using LC-MS/MS & NMR
Introduction: Why Identification of an Unknown Impurity is Critical in Phase 3 Drug Development In late-stage pharmaceutical development, identification of
Peptide Characterization Case Study: Identifying Sequence Impurities in a GLP-1 Analog
Introduction: The Role of Peptide Characterization in GLP-1 Analog Therapeutics In the development and QC stages of GLP-1 receptor agonists,
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E&L Testing CRO Case Study: Mitigating Leachables Risk in a Biologic Vial System
Introduction: Why Addressing Leachables Risk in a Biologic Vial System is Crucial In 2025, the biopharmaceutical industry continues to face
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