- Identification and quantification for surfactant and polymer
- Method Development of preservatives by HPLC method.
- Raw materials analytical method development for impurities and Assay
- Wastewater sample for trace element analysis by ICP-MS
- Determination of Heavy Metals at ppt levels by ICP-MS
- Product Release Rate and Membrane integrity test
- Dissolution comparative profiling of tablet, capsule and oral paste
- Capabilities to detect elemental impurities in water, beverages, wastewater, paint, toys, food, medicinal product.
Method Verification and Formulation Support
- Capsule, tablet, liquid, syrup, suspension, cream, ointment, lotion and Injectables
Analytical Method Development /Analytical Method Validation
- Analytical method development and Analytical method validation for Assay, Impurities, Content uniformity of active ingredients/excipients in pharmaceuticals, nutraceuticals
- Analytical method development to identify and quantitate active, excipients and preservatives in tablet, capsule, liquid, syrup, cream and ointment.
Regulatory Submission capabilities and QA services
- ANDA submission with US Agent Services
- NDS,ANDS, Establishment licence/Site licence for pharmaceutical, natural health product manufacturer and Importer
- Quality Assurance representation for a medical device industry (accomplished)
- Analytical Data review to evaluate data integrity