Experimental protocol design and methodological guidance for epidemiological studies
State-of-the-art statistical data analysis
Technical evaluations of infectious disease test systems by independent experts
Assistance fulfilling requirements for CE compliance, WHO prequalification, and FDA EUA
Scientific support in the development of diagnostic test systems and COVID-19 vaccines
High standards and professionalism
Diagnostic products that fully comply with European Medical Device Directives and bear the CE mark, indicating adherence to EU standards of health, safety, and environmental impact
Expertise from leading scientific institutions and universities, including in the United States, France, Turkey, and other countries
Collaboration with regional reference laboratories, including those with A2LA accreditation
Conclusion of a Material Transfer Agreement with the CDC for an HCV rapid test project
NIH license application pending to develop and produce point-of-care rapid diagnostic tests
