Unveiling a New Era of
AI-powered
Drug Development

Leverage Lunit’s proven AI technology and domain expertise to unlock transformative insights for patient stratification, derisking, and accelerating clinical trials or streamlining target identification.

Our portfolio of purpose-built solutions—Lunit SCOPE IHC Suite, SCOPE IO, and SCOPE GP—are designed to support biomarker-driven strategies for advancing emerging drug programs including antibody-drug conjugates, immuno-oncology therapies, or targeted small molecules.

Leading the Way: From Concept to Commercial

Proven regulatory track record

Proven regulatory track record

With three AI-based SaMDs successfully registered across the world including US, EU and 27 other countries—Lunit brings a proven global track record. Our dedicated regulatory affairs experts deliver customized strategies and help you navigate complex regulatory landscapes with confidence.

End-to-end support for clinical trial success

Ready for global clinical trial deployment and fully compliant with relevant standards, and fully resourced to provide required regulatory support, Lunit's solutions are built for AI-powered CDx development. Backed by an extensive clinical trial operations network including CRO partners, an expert pathologist network, and image/data sourcing, our team delivers trusted solutions at every stage.
End-to-end support for clinical trial success

Seamless path to global CDx commercialization

Deploy your AI-powered CDx at scale with a partner trusted by leading pharmaceutical organizations. With regulatory-cleared solutions in 65+ countries and integration-ready platforms, Lunit combines proven global reach with deep expertise in digital pathology and CDx commercialization.
Seamless path to global CDx commercialization

Collaborer avec les leaders mondiaux du secteur

A Trusted Partner to Power Your Next Breakthrough

Our AI models generate extensive data, and our internal biomedical research team and medical directors help navigate it to identify the most relevant data points to answer your scientific questions.

With an internal team of over 20 medical doctors and 50 AI researchers, Lunit is dedicated to developing clinically impactful AI solutions. Over the past 12 years, our cancer screening technologies have been adopted by more than 10,000 healthcare providers across 65+ countries, supporting confident clinical decisions every day.

Trusted by Clinical and Industry Leaders

Dépistage du cancer

They tell me: you’re finding the smallest

cancers we didn’t see before.

It’s making a real difference.” These successes have strengthened trust, increased referrals to their center, and directly benefited patients. Smaller cancers often mean less invasive treatment, lower costs, and better prognoses.

Dr Megha Gupta, médecin
Dr Megha Gupta, médecin
Radiologue spécialisé dans le sein et le corps, Sol Radiology, Victorville, Californie
Oncologie
This collaboration with Lunit underscores our commitment to advancing precision medicine in oncology. Tools like this will help to address unmet needs by optimizing diagnostic workflows for NSCLC patients and, ultimately, improve their outcomes.
Kristina Rodnikova
Kristina Rodnikova
Head of Global Oncology Diagnostics, Oncology Business Unit at AstraZeneca
Build What’s Next With AI That’s Ready Now

Build What’s Next With AI That’s Ready Now

Are you future-proofing your precision oncology strategy? Let's discuss how integrating AI pathology solutions can secure and transform your drug development journey.

Foire aux questions

Do you have experience of co-development for a customized solution?

Lunit has developed 12 total digital pathology tools in collaboration with life science companies, of which 4 were developed with biopharma companies. We are currently pursuing co-development in both early development and late development.