ABOUT US

Who We Are

The company, founded by pioneers of the rapid test industry, has developed a proprietary patented immunoassay platform enabling the development of qualitative and multiplex point of care diagnostics. Results are obtained in few minutes from a single drop of blood (or any other type of sample).

NG Biotech sells a range of CE marked rapid tests Worldwide. Product validations are performed in comparison to laboratory standard reference methods such as Elisa or HPLC. The company is ISO 13485:2016 certified.

Current production capacity is of more than 4 million tests per month.

At NG Biotech we support our partners’ Innovation meeting their screening and monitoring needs; we develop new solutions for their applications. Targeted areas are m-Health, Companion and Medical Diagnostics. We also cover Animal Health, Agriculture and Biodefense among others. We put our know-how and expertise in product development, manufacturing and product registration at your service.

Vision
To become one of the global leaders in rapid tests.

Missions
– NG Biotech develops, manufactures and markets in vitro diagnostics for screening, diagnosis, monitoring and prevention.
– We focus on urgency of decision making processes with rapid and easy to use tests providing quicker support to healthcare professionals and patients.

Founders

NG Biotech was founded in 2012 by 3 pioneers in rapid tests industry. The company capitalizes on the expertise of a great team to become a global leader in its industry.

Milovan Stankov Pugès Milovan Stankov Pugès
President & CEO
Milovan Stankov Milovan Stankov
Co-Founder & General Advisor
Biologist / Immunologist
Dr Alain Calvo Dr Alain Calvo
Co-Founder & General Advisor
PhD in Biology / Immunology

Facilities

Located in Guipry-Messac, France, NG Biotech, a pioneer in LFIA (Lateral Flow Immunoassay) technologies, operates a 5,000 m² industrial site that integrates all stages of product design, development, and manufacturing in compliance with international standards.

Quality

NG Biotech aims at providing products that meet customer and regulatory requirements, with the commitment to improve customer satisfaction through the effective application of NG Biotech’s quality management system.

NG Biotech Quality Management System is :

  • EN ISO 13485:2016 certified
  • MDSAP certified
  • compliant with Regulation (EU) 2017/746 (IVDR)

Our certifications cover the design, manufacturing and sales of in vitro diagnostic medical devices.