Review bioequivalence study report before send to regulatory to decrease the regulatory notes

We have R&D partner, and we can develop any products in our R&D/or in your site, also to do the stability batches and bioequivalence batch, follow up bioequivalence study, process validation, prepare/or review the registration file, be with you until your products ready for markets.

We have office in India for audit as 3rd party to any customer, also follow up any problem with Indian supplier, we can follow up your shipment and inspect the goods before shipping with documents