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GMP Certificates

GMP (Good Manufacturing Practice) is a core element of the quality management system that ensures the manufacturing and control of pharmaceutical products meet quality standards consistent with their intended use and the requirements of their registration dossier.

A GMP certificate confirms that the company’s manufacturing facilities and pharmaceutical quality system comply with EU GMP rules, PIC/S guidelines, and the World Health Organization’s GMP standards. It covers all requirements for production, trade, and distribution both in the domestic market and for export.

The Ukrainian pharmaceutical company InterChem SLC regularly confirms its compliance with GMP requirements through official certification:

  • 2007 – No. 15, dated 20.03.2007
  • 2009 – No. 9, dated 16.07.2009
  • 2011 – No. 10/2011/GMP
  • 2016 – No. 058/2016/SAUMP/GMP
  • 2019 – No. 051/2019/GMP
  • 2023 – No. 024/2023/GMP

The goal of GMP is to ensure the highest possible degree of safety, identity, and efficacy of medicinal products.

GMP represents a comprehensive set of standards and procedures strictly followed at the InterChem SLC manufacturing and laboratory complex. These standards must be applied at every stage of pharmaceutical production to guarantee the quality, safety, and effectiveness of medicines.