Global Pharma Analytics

Global Pharma Analytics (GPA) is a CGMP contract analytical chemistry laboratory. GPA provides a wide range of professional services to support pharmaceutical, medical device, nutritional and specialty chemical companies, from analytical testing and stability programs to consulting services. GPAs’ wealth of knowledge, experience in laboratory testing and regulatory guidance will ensure customers that our analysis are precise, accurate and above the industry standard. While GPAs’ is proficient in compendial analyses, including USP, EP, JP and AOAC methodologies, we also custom tailor analyses based on the individual customers' very unique analytical needs. We pride ourselves on providing the best in analytical troubleshooting for a wide variety of applications, while preserving a high standard of quality. Typical USP Chapters Tested by GPA Include: Identification-Organic Nitrogenous Bases, Identification Tests Identification by TLC Aluminum Limit Test Arsenic Limit Chloride and Sulfate Limit Dimethylaniline Ethylene Oxide and Dioxane Limit Heavy Metals Iron Lead Readily Carbonizable Substances Residue On Ignition Acid-Neutralizing Capacity Assay for Steroids Barbiturate Assay Epinephrine Assay Folic Acid Assay Iodometric Assay Residual Solvents Acetic Acid in Peptides Zinc Determination Alcohol Determination, Method IIa and IIb Color and Achromicity Completeness of Solution Deliverable Volume Disintegration Dissolution, Apparatus 1 & 2 Loss On Drying Loss on Ignition Optical rotation Osmolality and Osmolarity Particle Count Viscosity Water Determination, Method Ia only