Pharmaceutical Analysis

We offer

• Premier compliance record
• Well equipped facilities with critical mass and available buffer capacity
• Over 70,000 sq ft of area
• Experienced full time regular staff that understands your needs
• Partnership, responsive approach with strong emphasis on engaging you in consultative dialogue
• More than 20 years of experience in Pharmaceutical Industry

Capabilities

• Method Development and Validation
• Assays (Potency, Related Substances, Chiral, Preservatives, other components)
• Comparator studies
• Cleaning (Development, Validation & Testing for active and detergent residues)
• Analytical Support for Formulation Development
• Preclinical, excipient compatibility studies, prototype testing
• Stability and QC release testing
• Reference Standard Characterization
• API Characterization
• Isolation and identification of impurities
• Stability management and storage