Complete stability programme management service is provided as per ICH guidelines / special requirements in a cGMP and GLP compliant environment at our associated companies.
Provide analytical support in analytical method development / validation, Routine analyses of products by HPLC/GC/MS etc., Product characterization and Impurity profiling at our associate companies.
Total development of product from lab scale to pilot plant scale to actual production scale for Drug Substance and Drug product.
Business Development and Business consultancy is provided on various aspects related to Product Development and Contract Manufacturing both for Domestic and Export markets.
Monitoring and liaisoning with the CRO’s for PV or PhV (Pharmacovigilance Study Report) & BA/BE (Bioavailability/Bioequivalence) Studies Reports