Validation and qualification of critical facilities for the Life Sciences sector, through our own methodology, the result of more than 30 years of experience. COMSA Bio&Pharma technicians are specialized in the elaboration of protocols and reports according to ISO standards, GMP (Good Manufacturing Practices of the pharmaceutical industry), PICs (Pharmaceutical Inspector Convention Scheme), GLP (Good Laboratory Practices), FDA (Food and Drug Administration), Invima and MERCOSUR.