Garmen Laboratory

Garmen Laboratory provides complete pharmaceutical services to a broad range of industrial, institutional and governmental agencies. With nearly 35 ears of industry experience, Garmen provides a wide range of solutions that can answer all pharmaceutical, nutraceutical or cosmetics needs from formulation to testing release. We have a strict quality assurance program that meets 21CFR211 - GMP. In addition we are accredited by Health Canada and we are an FDA registred facility. We participate in round-robin performance evaluation studies. We consider ensuring the quality of work to be a prerequisite in serving our clients needs. Analytical Capabilities: • Chromatography 1.HPLC (UV, PDA, RI, Fluorescence, MS-MS, Dionex…) 2.GC (FID, ECD, µECD, MS…) 3.TLC • UV-VIS Spectrophotometry • Dissolution (Type I – VI) • Disintegration • Automatic Titrators • Karl Fisher Titrators • Atomic Absorption Spectrophotometry (AA) • ICP-MS Spectrophotometry • Fourier Transform Infrared Spectrophotometry (FTIR) • Particle Size Analysis Stability: • 25°C/60%RH • 30°C/65%RH • 40°C/75%RH • 2°C – 8°C • Light (controlled humidity) • Freeze-thaw cycling (-20°C to +200°C) Formulation Technologies: - Immediate release - Sustained and extended release - Direct compression - Dry or wet granulation - Spray drying - Extrusion/spheronization - Bi-layer tablets - Dry-coated tablets - Gastroretentive and Muco-adhesive systems