Development (Formulation, Scale-up, Method Development)

Analytical Instruments and Methods for Cleaning Validation

Cleaning Validation | Measurement of Drug Component Residues (Swab Method)

Analysis by ICP Atomic Emission Spectrometry in Accordance with the ICH Q3D Guideline for Elemental Impurities

Analysis of Decomposition Products in Drugs (LC/MS)

Analysis of Nitrosamines in Sartan-Type Bulk Drug Substances

Impurities and Foreign Matter | Analysis of Colored Components on the Surface of Pills (FTIR)

Impurities and Foreign Matter | Easy Elemental Analysis of Pills (EDX)

Quantitative Analysis of Trace Impurities in Drugs (LC/MS)

Simplified approach for structural elucidation and quantitation for pharmaceutical API and related impurities

LC/MS/MS Analysis of Impurities in Active Pharmaceutical Ingredients Using the Co-Sense for Impurities System

Method Transfer and High-Speed Analysis of Impurities of Drug by Prominence-i

Analysis of nitrosamine impurities according to USP General Chapter < 1469 >

Extractables & Leachables

High-Speed Analysis of Pramipexole following the Draft Guidance of International Harmonization of Pharmacopoeias

Analysis of Irbesartan Using an Integrated LC System - Nexera-i MT

Ultra-High Speed Analysis of Ibuprofen by Nexera in Accordance with USP 621

i-DReC, a New Photodiode Array Detector Function; Impurity Analysis Application

Recovery Test of Sodium Dodecylbenzenesulfonate by TOC-LCPH

15 Second Screening Analysis of Cyanide in Blood Serum Without Pretreatment

Technologies for Enhanced LC and SFC Workflow

Diffusion of Metal into Bone Tissue

Interactions between Benzoic Acid and Magnesium Oxide

Melting of Aspirin

Physical Properties and Observations | Internal Observations of Pills

Push-Out Test for Pills in Push-Through-Packs

Strength Testing of Pill Score Marks

Analysis of Residual Solvents in Drugs (Headspace GC)

GC Analysis Data Collection for Residual Solvents in Pharmaceuticals

GCMS Qualitative Analysis of Impurities Detected in Tests for Residual Solvents in Pharmaceuticals

Measurement of Residual Solvents in Pharmaceuticals by Headspace GC - USP <467> Residual Solvents Procedure A-

Simultaneous Analysis of Class 1, 2A and 2B Residual Solvents in Pharmaceuticals via HS-GCMS

Analysis of Residual Solvents in Pharmaceuticals Using Headspace GC-FID/MS Detector Splitting System

Analysis of Residual Solvents in Pharmaceuticals by Water-Soluble Samples Using N₂ Carrier

Analysis of Residual Solvents in Pharmaceuticals by Nexis GC-2030 + HS-20 (JP17 Supplement II, USP 467)

Analysis of Residual Solvents According to the New ICH Q3C Guideline