European Laboratory holding MIA license as well as GMP certificate and serving Pharma Industry with EU Batch Release Testing, QP Batch Release, and Product Development. 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 the drug product life cycle, starting from early development and drug registration to routine commercial supply for the EU market. We help to assure product quality by performing QC testing and opening doors to complex European markets.