TECHNOLOGY

Varifarma has recently incorporated a new facilities for final formulation of solid. This new pharmaceutical plant will produced the forms of tablets, covered tablets and rigid capsules with citoestatic active principles and their corresponding packaging in blisters.

These areas respond to the present requirements of Good Practices of Manufacture (GMP) as far as surfaces, ceiling, illumination and air supplies.

It has systems of aspiration, dust retention, and its air conditioning and instruments to the measurement of the pressure differentials.

It count qualifications of installation and operation of the air system, the system of water treatment, of the equipment of production and the calibration of instruments for the process control.

Our Standard Operation Procedures (SOP) guarantees the quality of the different operations and with it the quality of products elaborated by the laboratory.

Quality assurance

The laboratory counts with an area of quality assurance destined to the emission and fulfillment of the necessary documentation according to the sanitary exigencies.

Also is in charge of internal auditories, continuous qualification to the personnel, verifications in all the inherent sectors of the plant to the production areas, control of quality, of the deposits ding it´s main objectives to assurace.

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