Ekvitestlab

Focusing on the needs of users and the latest scientific research, we are constantly working on expanding the range of our products and improving the analytical and diagnostic characteristics of ELISA kits, as well as their stability. The company’s professional team ensures sustainable production of a complete list of “EQUI” brand ELISA kits and works to meet the needs of the medical products market with high-quality diagnostic systems. The company ensures an uninterrupted supply of products and provides comprehensive service support for its users.
The company’s implemented and certified quality management system in accordance with ISO 13485:2016 ensures compliance of ELISA kits with the high requirements of standards for product quality. Production undergoes regular audits to assess product compliance with the requirements of the Technical Regulation on medical devices for in vitro diagnostics, which is confirmed by relevant certificates issued by the competent body for assessing compliance.

In 2021, the company began the process of product certification in accordance with the requirements of European legislation. Having successfully passed all stages of inspection of production and products for compliance with Directive 98/79/EC of the Council of the European Union, it received the right to apply CE marking to a significant list of products and continues to confidently move towards expanding the list of ELISA kits with CE marking in accordance with the Regulation of the European Parliament and of the Council (EU) 2017/746, which confirms the unchanged quality of “EQUI” trademark products and opens up new opportunities for international cooperation.