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To perform analytical method development of drug products for different tests like Assay/Dissolution/Degradation products/Residual solvents/water content by using advanced techniques like HPLC/GC/UV/KF
To perform documentation through the BIOVIA system to ensure data integrity, traceability, version control, audit trail compliance, and secure electronic record management in accordance with applicable quality and regulatory requirements.
Performing routine/initial analysis of drug products for market samples/query response.
Preparation of method development protocols, reports, method equivalency report and COA
To perform multimedia dissolution study and compatibility study and prepare report of the same.
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