The manufacture of vaccines and pharmaceutical products is strictly and legally regulated. These rules require the installation of appropriate facilities and production processes carried out under an accredited quality assurance system.

Our Quality System covers the following areas:

Ongoing staff training in quality assurance.

Ongoing staff training in GMP (Good Manufacturing Practices) and GLP (Good Laboratory Practices).

Procedures and protocols for manufacturing processes and control.

Specific documentation for each batch.

Reference/ retention samples

Quality Control audits.

Process and Equipment validations

The manufacture of biological products takes place in controlled environments. All the systems, production processes and equipments are regularly subjected to validations in order to fully comply with the defined specifications.

CZV is certified by the Spanish Agency for Medicines and Health Products  in compliance with the regulations for Good Manufacturing Practices (or GMP) of veterinary products.

This GMP certification is recognized across Europe and internationally by the respective governmental bodies.

The Quality System of CZV is approved and certified by numerous official organizations, as well as by our own customers over five continents.

At CZV, we develop our work with a firm commitment to and an absolute respect for the environment.

CZV fully complies with all applicable European Union environmental regulations (waste management, air emissions, treatment of liquid effluents, etc.).