• Orthogonal Separation of Pharmaceutical Impurities
• Development and Verification of a Generic Agilent 1260 Infinity II Binary HPLC Method - Simultaneous separation and quantification of  seven OTC drugs
• Identification of Common Excipients and APIs Through Blue Drums
• The Expert's Guide to Pharmaceutical Impurity Analysis
• Analysis of Risedronate According to USP Using the Agilent 1260 Infinity Bio-inert Quaternary LC System

Looking for more resources to advance your analytical workflows for drug characterization applications? Visit our Drug Characterization page.

• Quantitation of N-Nitroso Nebivolol in Nebivolol Tablet Formulation
• Quantitation of N-Nitroso Hydrochlorothiazide in Losartan Hydrochlorothiazide Tablets
• Quantitation of N-Nitroso Moxifloxacin in 400 mg Moxifloxacin Tablet Formulation
• Quantitation of N-Nitroso Dabigatran Etexilate Impurity
• Determination of Nitrosamine Impurities Using the Agilent 6495 Triple Quadrupole LC/MS System
• Improved LC/MS Performance for the Determination of Polar Nitrosamines by Means of the Agilent 1260 Infinity II Hybrid Multisampler
• Quantification of Nitrosamine Impurities in Sartan Drugs Using an Agilent GC/TQ with Hydrogen Carrier Gas
• Quantitation of N-Nitroso N-Desmethyl Diphenhydramine in Diphenhydramine HCl API
• Quantitation of N-Nitroso Sitagliptin Impurity (NTTP) in Drugs by Agilent 6475 LC/TQ
• Improved LC/MS Performance to Determine Polar Nitrosamines Using the Agilent 1260 Infinity II Hybrid Multisampler
• Simultaneous Estimation of Eleven Nitrosamine Impurities in Metformin Drug Product Using an Agilent 6495D LC/TQ

Looking for more resources to advance your analytical workflows for mutagenic impurities analysis applications? Visit our Mutagenic Impurities Analysis page.

• Analysis of Volatile Compounds Identified in Rubber Gasket Extracts Using GC/MSD and High-Resolution GC/Q-TOF 

Looking for more resources to advance your analytical workflows for E&L analysis applications? Visit our Extractables and Leachables Analysis page.

• Modernizing LC Methods for USP Phenylephrine HCl and Pramoxine HCl in OTC Products
• USP Method Transfer from the Agilent 1100 Series Quaternary LC to the Agilent 1260 Infinity III LC
• Modernizing the USP Acetaminophen and Caffeine Tablets HPLC Method Following the Revised USP <621> Guidelines
• Modernizing the USP Ceftizoxime Sodium HPLC Method Following the Revised USP Guidelines
• Useful Strategies for Modernizing USP Methods
• Reduced Solvent Use and Analysis Time According to USP Methods
• Reduce the Cost per Injection for Your USP Compendial Method

Looking for more resources to advance your analytical workflows for revisions per USP <621> applications? Visit our Revisions to Analytical Procedures per USP <621> page.

• LC/MS/MS Method for the Low-Level Quantitation of Fluticasone Furoate in Plasma
• Illuminating the Cellular and Molecular Response to Drug Treatment by Combining Bioenergetic Measurements with LC/MS Omics 

Looking for more resources to advance your analytical workflows for ADME/pharmacokinetics and bioanalysis applications? Visit our ADME/Pharmacokinetics and Bioanalysis page.

• Rapid, Image-Based Viability and Outgrowth Analysis for Neurotoxicity Assays
• Multiplexed Assessment of Mitochondrial Function Combining the Agilent Mito-rOCR Assay with Live-Cell Imaging
• Assessing NK Cell Bioenergetic Metabolism Using Extracellular Flux Analysis 
• Accurate Assessment of Metabolic Reprogramming During Adipocyte Differentiation
• Discovery of a New Inhibitor for PFKFB2 Kinase Activity Through Mechanistic Studies

Looking for more resources to advance your analytical workflows for cell analysis and drug toxicity applications? Visit our Cell Analysis and Drug Toxicity pages. 

• Regulatory Compliance with Agilent ICP-MS MassHunter and OpenLAB Server
• Regulatory Compliance with Agilent ICP-MS MassHunter and OpenLab ECM Software
• Support for Title 21 CFR Part 11 and Annex 11 compliance: Agilent MassHunter GC/MS Software Products

Looking for more resources to advance your analytical workflows for compliance support and services applications? Visit our Compliance Support and Services page.

• Method Transfer from an Agilent 1100 Series Quaternary LC to an Agilent 1260 Infinity II LC
• Method Transfer from an Agilent 1100 Series LC to an Agilent 1260 Infinity II LC
• Analyzing Iohexol by Compendial Method Produces Excellent Precision with Shallow Gradients Using the Agilent 1260 Infinity III LC
• Accurate Robust Accelerated Analytical LC Method Development InfinityLab LC Solutions
• Method Verification of the United States Pharmacopeia Monograph with the Agilent Cary 60 UV-Vis

Looking for more resources to advance your analytical workflows for method development applications? Visit our Pharmaceutical Method Development page.

• Entire Workflow from Dissolution Sampling, LIMS, HPLC Measurement to Result
• Automating Dissolution Testing with an Agilent Online LC System

Looking for more resources to advance your analytical workflows for dissolution testing applications? Visit our Dissolution Testing page.

• Residual Solvents Analysis for the Pharmaceutical Industry Using the Agilent 8697 Headspace Sampler and 8850 GC-FID System

Looking for more resources to advance your analytical workflows for residual solvent analysis applications? Visit our Residual Solvent Analysis page.

• Analysis of Extractable and Leachable Metals in Plastic Materials used for Drug Products by ICP-OES
• Analysis of Artificial Tear Eye Drops For Elemental Impurities

Looking for more resources to advance your analytical workflows for elemental impurities analysis applications? Visit our Elemental Impurities Analysis page.

• Supporting Continuous Manufacturing of Drug Products with Transmission Raman Spectroscopy
• Quantification and Identity Testing of Soft Gel Capsules using Transmission Raman Spectroscopy
• Quantification of Tablets Containing Multiple APIs Using Transmission Raman Spectroscopy
• Supporting Continuous Manufacturing of Drug Products with Transmission Raman Spectroscopy 

Looking for more resources to advance your analytical workflows for content uniformity applications? Visit our Solid Dose Testing page.

• Quantitative Determination of Salt-Form Impurities of Warfarin at the Lowest Commercial Dose Strength using Transmission Raman Spectroscopy

Looking for more resources to advance your analytical workflows for polymorph analysis applications? Visit our Solid Dose Testing page.