About

About Profarma Europe based EU GMP certified and MIA License holding Laboratory ensuring patient safety by testing pharmaceutical products, developing new medicines, and performing QP batch release to the EU market together with pharma manufacturers and distributors. Profarma‘s expertise includes small molecules, peptides, and biologics, including active pharmaceutical ingredients (API), intermediate stages, and final drug products. Our clients come to us at different stages of drug product life cycle starting from early development, drug registration to routine commercial supply for EU market. We help to assure products quality and open doors to complex European markets. About Profarma Europe based EU GMP certified and MIA License holding Laboratory ensuring patient safety by testing pharmaceutical products, developing new medicines, and performing QP batch release to the EU market together with pharma manufacturers and distributors. Profarma‘s expertise includes small molecules, peptides, and biologics, including active pharmaceutical ingredients (API), intermediate stages, and final drug products. Our clients come to us at different stages of drug product life cycle starting from early development, drug registration to routine commercial supply for EU market. We help to assure products quality and open doors to complex European markets. Europe based EU GMP certified and MIA License holding Laboratory ensuring patient safety by testing pharmaceutical products, developing new medicines, and performing QP batch release to the EU market together with pharma manufacturers and distributors.