The quality system is the means to ensure the quality of operations etc. like that affect compliance with the requirements. The quality system binds together requirements imposed and the conformity to those requirements and conformity analysis to source materials, production process,end product, employees, premises, equipment and other factors influencing the quality directly or indirectly. The company's Management Board is convinced that the quality of the product depends on each employees contribution to that and at the same time ensuring the quality of the product must be organized in a good teamwork.
TFC-s activities include:
• human medicinal products manufacturing and wholesale;
• veterinarian medicinal products manufacturing and wholesale;
The entire production process (purchase of materials, production, quality control and release and marketing) meets to the requirements of Good Manufacturing Practice.
As from year 1998, the company has implemented a quality management system according to series of standards of ISO 9000. In December 2015 the international auditing company Bureau Veritas Certification issued the quality management system certificate No. EST104615A, according to which the manufacturing and technological development surface of semi-solid and liquid dosage forms in TFC is in accordance with requirements of ISO 9001:2008. The certificate is valid for three years (15.09.2018), during which there are regular supervision audits.