GMP Compliance

Solvias has been duly authorized by Swissmedic, the Swiss Agency for Therapeutic Products, to manufacture medical products. This authorization allows Solvias to perform pharmaceutical analyses and to manufacture active pharmaceutical ingredients (API) for use in clinical trials within the standard of Good Manufacturing Practice (GMP). The certificate is based on inspections performed in accordance with the requirements of good practice in manufacturing and quality control of the Pharmaceutical Inspection Convention/Cooperation Scheme (PIC/S) and the Directives of the European Commission.