Arman Shimisanj Pharmaceutical Analysis Department
The drug analysis laboratory of Arman Shimisanj Company began providing services as a quality control and pharmaceutical research laboratory in 1400 and, by benefiting from ISO17025 standards, GLP requirements, and Food and Drug Administration licenses, has been able to provide customers with desirable services as a laboratory partner in the pharmaceutical industry. This laboratory is equipped with chemical measurement devices such as gas chromatography, high-performance liquid chromatography, ultraviolet and visible spectrophotometer, infrared spectrophotometer, titrator, tablet dissolution device, atomic absorption and emission, etc.
The testing laboratory conducts tests according to the latest guidelines, including the authoritative pharmacopoeias USP, BP, EP, or the manufacturer’s in-house method.
The availability of an ultra-sensitive balance (seven decimal places) has reduced the standard sample amount required for analyses to less than 1 milligram. The USP Minimum Weight for weighing in this company, in accordance with USP requirements, is 0.5 milligrams.
Also, our colleagues in the documentation department provide customers with all analysis documentation, including chromatograms, spectra, balance weighing printouts, and other analytical data, along with the certificate of analysis, to ensure the accuracy of information and compliance with data integrity.
This laboratory has the ability to perform the following tests:
- Assay percentage test of active pharmaceutical ingredient
- Uniformity of dosage test
- Dissolution
- Impurity and related compounds
- Residual solvents
- Tests on alcohols and alcohol-based and benzalkonium chloride-based disinfectants
- water determination
- Optical Rotation
- Chemical Testing
- Residue on Ignition
- Loss on Draying
- Heavy metal measurement
- IPQC Tests
