Arman Shimisanj Drug Analysis Laboratory, as a reference drug analysis laboratory approved by the Food and Drug Administration and holding the relevant permits, is proud to offer drug analysis services to its valued clients.

Utilizing instrumental analysis equipment and an ultra-microbalance (seven decimal places), this laboratory provides pharmaceutical analyses to its clients with the minimal consumption of reference standards.

All analytical methods comply with reputable pharmacopoeias such as USP, BP, EP, JP, etc., and are performed according to validated internal methods based on client needs. All analysis documents and records, such as weighing prints, chromatograms, spectra, calculations, etc., will be provided to the client along with the relevant drug analysis certificate.

The pharmaceutical analyses performed by this company include the following:

Qualitative Analyses

• Identification via Infrared and Ultraviolet Spectroscopy

• Chemical Identification Tests

• Physical Identification Tests (Melting Point, Boiling Point, etc.)

Quantitative Analyses

• Determination of Active Pharmaceutical Ingredient (API) Percentage (Assay)

• Tablet Dissolution in Three Release Profiles (Sustained, Delayed, and Immediate)

• Pharmaceutical Impurities (Organic Impurities)

• Residual Solvents

• Dosage Uniformity of the Active Ingredient (Uniformity of Dosage Units)

• In-Process Quality Control (IPQC) Analyses

• Sample Water Content (Loss on Drying/Karl Fischer)

Arman Shimisanj Laboratory is equipped with Liquid Chromatography (HPLC with RID, PDA, UV detectors), Gas Chromatography (GC with FID, Mass Spectrometry), Molecular Spectrophotometers, Titrators, and Karl Fischer apparatus.