Capabilities

 CADD performs a wide range of assays to obtain data for pre-approved
active pharmaceutical ingredients, new molecular entities,
drug products and excipients. These include:

	Stability-indicating assay development and method validation
	Technical transfer of analytical methods
	API/excipient monograph testing
	Quality control analysis
	Preformulation studies
	Dissolution methodology and assay development, followed by validation
	In-Vitro testing of dosage forms
	Long-term stability studies
	Information as per regulatory guidelines for document preparation and submission