Your trusted CDMO partner with expeditious timelines that help to reduce the client efforts to scout for products by providing comprehensive integrated solutions right from selection to filing

Etico was established by a team of seasoned professionals with a mission to develop and produce innovative, high-quality medicines. As a US FDA-registered company (FEI No: 3013758337 & DUNS No: 67-546-6037) with ISO 9001:2015 certification, DCA (Form 37) approval, and recognition as a GLP and DSIR-certified research organization, we specialize in the development of generics, generic plus, and controlled release products across multiple therapeutic areas and dosage forms.