At Globesynth Pharma Tech, we transform complex chemistry into reliable pharmaceutical solutions. Our core strength lies in industrial organic synthesis and the development of high-quality, traceable working standards, supporting pharmaceutical innovation from early research through commercial manufacturing.
We partner with our clients to deliver precision, consistency, and regulatory confidence at every stage of product development.
Our traceable working standards are meticulously synthesized and comprehensively characterized to serve as trusted reference materials for impurity identification, quantification, and control in APIs and finished dosage forms. Designed to meet global regulatory expectations, our standards help ensure product safety, analytical accuracy, and compliance
Accurately detect and quantify process-related impurities, degradation products, and residual solvents, ensuring impurity profiles remain within approved limits.
Each standard is supported by clear traceability aligned with ICH, USP, and Ph. Eur. guidelines, giving you confidence in data integrity and reproducibility.
Delivered with complete analytical support including NMR, HPLC, LC-MS, and GC, confirming identity, purity, and structural correctness.
Developed in accordance with ICH Q3A/Q3B requirements, our standards are suitable for method validation, stability studies, and regulatory submissions such as ANDAs and DMFs.
From rare organic impurities to elemental and residual solvent standards, we offer custom synthesis solutions tailored to your specific molecule and project timelines.
With a commitment to quality, transparency, and scientific excellence, Globesynth Pharma Tech delivers impurity standards you can trust—helping you accelerate development, reduce risk, and achieve regulatory success worldwide.