Raw Material Testing
- API (Active Pharmaceutical Ingredients) and excipients analysis
- Identification, purity, and impurity profiling
- Physical and chemical characterization
Finished Product Testing
- Compliance with pharmacopoeial specifications (IP, BP, USP, JP, Martindale’s)
- Evaluation of dosage form uniformity, content, and stability
- Testing for dissolution, disintegration, hardness, and friability
Stability Studies & Shelf-Life Testing
- Testing under various climatic conditions
- Determining potency, degradation, and impurity levels over time
Microbiological Testing
- Sterility testing of injectable & ophthalmic products
- Endotoxin testing & microbial limit analysis
Elemental & Heavy Metal Analysis
- Detection of toxic metals (Arsenic, Lead, Mercury, Cadmium, etc.)
Residual Solvents & Impurity Profiling
- Identification of solvents, contaminants, and degradation products
Finished Pharmaceutical Products We Test
- Oral Liquids & Solids – Syrups, suspensions, emulsions, tablets, capsules, and powders
- Topical Semi-Solids – Ointments, gels, creams, and lotions
- Ophthalmic Products – Eye drops and sterile ophthalmic solutions
- Parenteral Products – Injectable formulations, including IV solutions and sterile powders
- Aerosols & Inhalation Products – Metered-dose inhalers (MDIs), dry powder inhalers (DPIs), and nebulizers
