The company's production complex Orisil-Pharm systematically undergoes inspection by the State Service for Medicines. As a result of the last inspection, we received a Certificate of Compliance with the Production Conditions Requirements GMP.

This is another huge victory that the entire company team is proud of. Orisil-Pharm, because we have been going to this for 10 years. This is a long path of hard work, self-development, as well as significant investments in production facilities, their improvement and modernization. We never stop at what we have achieved. After all, such events give even more strength and inspiration to work and develop for the benefit of society.

Brief description of the international standard GMP.
Standard Good Manufacturing Practice (trans. from English – good manufacturing practice) – a set of rules and regulations that describe the requirements for production activities and quality control of medicines, biologically active supplements, food products, medical devices, and diagnostic products.

Standard GMP intended for:

  • ensuring an excellent level of quality and reliability of manufactured products
  • guarantees that the drug is made according to the same formula as declared for production
  • does not contain third-party applications
  • labeled and packaged as required
  • does not lose its properties during the shelf life.

This international standard sets requirements for the quality management system, personnel management, requirements for the equipment used and production buildings, as well as requirements for document management. Everything must meet the highest quality requirements.