Geeng builds Software as a Medical Device (SaMD) for molecular biology laboratories. Our work operates within the EU IVDR 2017/746 regulation, with development practices aligned to IEC 62304 (medical device software lifecycle) and ISO 14971 (risk management).

Our conviction: diagnostic software should never add friction to a biologist's work. It should make complexity legible, without ever compromising on the reliability of the result.

PCRHub — A platform for PCR and digital PCR (dPCR) analysis, designed to simplify the interpretation of molecular biology results in routine laboratory use.

DIAGNOW — A genomic data interpretation platform, turning raw sequencing data into clinically actionable information.

We build in an environment where traceability, validation, and risk management are not afterthoughts but design constraints from day one. This shapes our architecture choices, our third-party dependency management, and our testing practices — with one constant goal: keeping software innovation compatible with medical device requirements, without slowing down how fast we respond to the real needs of biologists.