Complete assistance to be provided from documentation to final procurement for all  API grades (USP/ CEP/BP) that are suitable for user-friendly dosage forms.

Development includes high screening, scanning  and optimization of  favorable formulations and processes.

All types of regulatory submissions (CTD/ eCTD) from semi regulated to high regulated markets.

Complete analytical support services starting from method development and validation, reverse engineering, microbiological services , stability studies, characterization and technology transfer.

Managing identifying site to audit compliance.