Bio&Pharma areas of activity

Comprehensive projects for the life sciences & technology sector

Development and projects’ execution

Qualification and validation

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.

After-sales service and maintenance

COMSA Bio&Pharma offers an After-Sales service with specialists who facilitate diagnosis, development, periodic controls and validation of critical areas, with the possibility of specialized 24/7 full-service contracts for industries in the Life Sciences sector.

GMP Compliance ServiceS

Based on more than 40 years of experience in the Life Sciences sector, COMSA Bio&Pharma offers the conceptualization of projects for this sector, following current regulations and the most innovative solutions in the industrial world.