The depth and breadth of the analytical services can support all phases of drug discovery and development studies. We offer our clients the added advantage of competence under GLP.  Validation is conducted according to FDA-ICH guidelines, client approved protocols and Standard Operating Procedures.

• Develop analytical methods for drug substances and pharmaceutical products

• Assay procedures for drug product

• Assay procedures for dissolution samples

• Establish drug criteria

• Full range of method validations that conform to regulatory and customized client requirements

• Full inter-laboratory transfer

Quality analysis and control