22-05-2023

hema.to closes its seed round

We closed our €3.6M round, led by Elaia Partners

End of May, we closed our seed round with Elaia Partners, heal capital and HTGF to bring precision diagnostics to immune medicine. Anne-Sophie Carrese says, about the deal: "We have been convinced by the founding team, composed of three former entrepreneurs from the same company, with three PhD profiles, at a stage where they are going to scale their go to market, which is coherent with our deep tech seed investment thesis", Managing Partner at Elaia Partners. See tech.eu's press release here.

15-10-2022

hema.to is FDA compliant

In record time ...

.. we've achieved FDA-compliance (as a class I device) less than four months after receiving our CE mark. This was made possible by the professionalism and dedication of our team, but in particular by our US regulatory partner QServe Group, and our contact Jennifer Hadfield (left in picture), and our EU regulatory partner Be-on-Quality. The picture shows Aleks and Jennifer registering our device; the following day the FDA sent us the good news.

20-09-2022

Clinical study published

Clinical trial reveals hema.to is faster and better

We're incredibly proud to share that hema.to has been clinically validated in an international, four-center clinical trial! Blood cancer diagnoses weren't just twice as fast, they were made with 8% more sensitivity and 10% more specificity when made with the help of our beautiful, easy-to-use decision-support software. You can download the press release here.

14-07-2022

Medical Valley first prize

hema.to won the first prize ...

... at the Medical Innovation Night in Nürnberg, where we pitched hema.to in front of an audience an an excellent jury consisting of Medical Valley EMN e. V., Siemens Healthineers, aescuvest, GWQ ServicePlus AG, IONOS andFraunhofer IIS. We'll be using our E20k prize money to explore partnerships with GWQ and Siemens Healthineers.

26-05-2022

hema.to receives its CE mark

After months of hard work ...

... we are now compliant with the IVDD. We conform to ISO 13485 (quality management), ISO 14971 (risk management), ISO 62366 (usability), ISO 62304 (software life-cycle management) and IEC 82304 (health software).

Blog

Detecting small malignant B-cell populations in the blood and bone marrow using machine learning
September 27, 2024

Detecting small malignant B-cell populations in the blood and bone marrow using machine learning

Our cutting-edge AI model combines supervised and clustering approaches to detect small pathological B-cell populations in blood and bone marrow samples. Key features include:

  • Efficient identification of populations as small as 3% of total cells
  • Differentiation of 6 B-cell neoplasms (CLL, MCL, HCL, FL, MZL, DLBCL)
  • Ability to detect previously unnoticed secondary B-NHL clones
  • Optimized for low false negative rate, enabling fast and automated screening

This AI-powered tool offers systematic, rapid analysis, making it an invaluable aid for clinical B-cell neoplasm flow cytometry analysis in your laboratory. You can download the poster here.

We closed our €3.7M round, led by Elaia Partners
May 22, 2023

We closed our €3.7M round, led by Elaia Partners

End of May, we closed our seed round with Elaia Partners, heal capital and HTGF to bring precision diagnostics to immune medicine. Anne-Sophie Carrese says, about the deal: "We have been convinced by the founding team, composed of three former entrepreneurs from the same company, with three PhD profiles, at a stage where they are going to scale their go to market, which is coherent with our deep tech seed investment thesis", Managing Partner at Elaia Partners. See tech.eu's press release here.

hema.to is FDA compliant in record time ...
October 15, 2022

hema.to is FDA compliant in record time ...

.. we've achieved FDA-compliance (as a class I device) less than four months after receiving our CE mark. This was made possible by the professionalism and dedication of our team, but in particular by our US regulatory partner QServe Group, and our contact Jennifer Hadfield (left in picture), and our EU regulatory partner Be-on-Quality. The picture shows Aleks and Jennifer registering our device; the following day the FDA sent us the good news.

Clinical study reveals hema.to is faster and better
September 20, 2022

Clinical study reveals hema.to is faster and better

We're incredibly proud to share that hema.to has been clinically validated in an international, four-center clinical study! Blood cancer diagnoses were made twice as fast and at clinical-grade when made with the help of our beautiful, easy-to-use decision-support software. You can download the press release here.

hema.to won the Medical Valley first prize ...
July 14, 2022

hema.to won the Medical Valley first prize ...

... at the Medical Innovation Night in Nürnberg, where we pitched hema.to in front of an audience an an excellent jury consisting of Medical Valley EMN e. V., Siemens Healthineers, aescuvest, GWQ ServicePlus AG, IONOS andFraunhofer IIS. We'll be using our E20k prize money to explore partnerships with GWQ and Siemens Healthineers.

hema.to receives its CE mark
May 26, 2022

hema.to receives its CE mark

... we are now compliant with the IVDD. We conform to ISO 13485 (quality management), ISO 14971 (risk management), ISO 62366 (usability), ISO 62304 (software life-cycle management) and IEC 82304 (health software).

Frequently Asked Questions

See more FAQ
What training resources are available for hema.to?
What kind of support does hema.to offer?
Can I adjust the results after the automated data analysis?
Should I use a specific cytometer / panel / workflow?
How many files per disease do the algorithms need in order to be trained?