Our laboratory services for Pharmaceutical Producers are conducted under GMP (Good Manufacturing Practice) certification, ensuring full regulatory and quality compliance for medicinal products.
Advanced Instrumental Methods
High-resolution analysis using HPLC, GC, UV-Vis, and ICP-OES for active ingredients, impurities, excipients, and finished pharmaceuticals. Supports method development, validation, and transfer in accordance with pharmacopeial standards.
API & Raw Material Testing
Comprehensive testing for identification, purity, potency, and elemental impurities (ICH Q3D). Essential for supplier qualification and batch release.
Batch Release Testing
Complete analytical panels for potency and uniformity testing. Certified results for regulatory submissions and market release within the EU, USA, and global markets.
Physical-Chemical Testing
Measurement of viscosity, pH, and other critical parameters.
Heavy Metals & Elemental Impurities
ICP-OES testing for regulatory compliance with strict EMA/FDA/ICH Q3D limits.
Water Quality Testing
Analysis of pharmaceutical-grade water (purified, WFI, process water) for chemical parameters.
Everything you need to know about our laboratory, services, and certifications.
No. Dietary supplements are analyzed according to ISO 17025 to ensure precision and transparency in food-grade products, while pharmaceuticals are tested under GMP (Good Manufacturing Practice) to meet strict pharmaceutical regulatory requirements.
Yes. Our laboratory provides complete batch release testing in compliance with GMP, including potency, purity, and analytical documentation for regulatory submissions and market release.
We test a wide range of pharmaceutical products — including tablets, capsules, excipients, and intermediates — all under certified GMP conditions.
