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Medical

GT BIOPHARMA ANNOUNCES FDA DATA - GTB-3550, FOR TREATMENT OF HIGH-RISK MYELODYSPLASTIC SYNDROMES

GT Biopharma | December 23, 2020

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GT Biopharma, Inc. (OTCQB: GTBP) (GTBP.PA) an immuno-oncology organization focused in on innovative treatments dependent on the Company's restrictive NK cell engager (TriKE™) innovation stage is satisfied to report the introduction of extra interval information results for the Company's lead therapeutic competitor, GTB-3550, for the treatment of high-risk myelodysplastic syndromes (HR-MDS). Erica Warlick, M.D, Principal Investigator for the GTB-3550 clinical trial, i...

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STEMCYTE SUBMITTED ITS APPLICATION FOR A BIOLOGICS LICENSE (BLA) FOR ITS PRODUCT "HPC-CORD BLOOD" TO THE US FDA

Stemcyte | March 23, 2022

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On January 7th, 2022, the FDA received the BLA (Biologics License Application) for the "HPC-Cord Blood" product. On March 8th, 2022, StemCyte was formally informed that the submission was acceptable to join the biologics license quality review process. The "HPC-Cord Blood" is an umbilical cord blood hematopoietic stem cell product intended for unrelated donor hematopoietic progenitor cell transplantation procedures in patients with hematopoietic system disorder...

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Industrial Impact

ACHIKO AG REPORTS BREAKTHROUGH CALIBRATION RESULTS FOR ITS APTAMEX™ COVID-19 RAPID TEST TECHNOLOGY

Achiko AG | January 15, 2022

news image

Achiko AG is pleased to report that new optimizations during recent calibration testing of its affordable, non-invasive Covid-19 saliva-based rapid test AptameX™ correctly differentiated 100% of test samples up until a comparable reverse transcription polymerase chain reaction cycle threshold value of 33, indicating the system’s ability to deliver a > 97% sensitive and > 97% specific rapid test at a wider range of viral loads than most other rapid tests. <...

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ARBOR VITA LAUNCHES OPEN PLATFORM COVID-19 ANTIBODY TEST EXPANDING ACCESS TO HIGHER QUALITY DIAGNOSTICS

Arbor Vita | June 08, 2020

news image

Arbor Vita announced today the availability of its CoVisa™ IgG ELISA-based test for antibodies associated with the novel coronavirus (COVID-19). The test has been found to have a 100 percent sensitivity (positive percentage agreement), and 99.24 percent specificity (negative percentage). Additional validation testing is ongoing in independent laboratories. The company has notified the U.S. Food and Drug Administration under the Emergency Use Authorization (EUA) process.Arbor Vita'...

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Medical

GT BIOPHARMA ANNOUNCES FDA DATA - GTB-3550, FOR TREATMENT OF HIGH-RISK MYELODYSPLASTIC SYNDROMES

GT Biopharma | December 23, 2020

GT Biopharma, Inc. (OTCQB: GTBP) (GTBP.PA) an immuno-oncology organization focused in on innovative treatments dependent on the Company's restrictive NK cell engager (TriKE™) innovation stage is satisfied to report the introduction of extra interval information results for the Company's lead therapeutic competitor, GTB-3550, for the treatment of high-risk myelodysplastic syndromes (HR-MDS). Erica Warlick, M.D, Principal Investigator for the GTB-3550 clinical trial, i...

Read More
news image

STEMCYTE SUBMITTED ITS APPLICATION FOR A BIOLOGICS LICENSE (BLA) FOR ITS PRODUCT "HPC-CORD BLOOD" TO THE US FDA

Stemcyte | March 23, 2022

On January 7th, 2022, the FDA received the BLA (Biologics License Application) for the "HPC-Cord Blood" product. On March 8th, 2022, StemCyte was formally informed that the submission was acceptable to join the biologics license quality review process. The "HPC-Cord Blood" is an umbilical cord blood hematopoietic stem cell product intended for unrelated donor hematopoietic progenitor cell transplantation procedures in patients with hematopoietic system disorder...

Read More
news image

Industrial Impact

ACHIKO AG REPORTS BREAKTHROUGH CALIBRATION RESULTS FOR ITS APTAMEX™ COVID-19 RAPID TEST TECHNOLOGY

Achiko AG | January 15, 2022

Achiko AG is pleased to report that new optimizations during recent calibration testing of its affordable, non-invasive Covid-19 saliva-based rapid test AptameX™ correctly differentiated 100% of test samples up until a comparable reverse transcription polymerase chain reaction cycle threshold value of 33, indicating the system’s ability to deliver a > 97% sensitive and > 97% specific rapid test at a wider range of viral loads than most other rapid tests. <...

Read More
news image

ARBOR VITA LAUNCHES OPEN PLATFORM COVID-19 ANTIBODY TEST EXPANDING ACCESS TO HIGHER QUALITY DIAGNOSTICS

Arbor Vita | June 08, 2020

Arbor Vita announced today the availability of its CoVisa™ IgG ELISA-based test for antibodies associated with the novel coronavirus (COVID-19). The test has been found to have a 100 percent sensitivity (positive percentage agreement), and 99.24 percent specificity (negative percentage). Additional validation testing is ongoing in independent laboratories. The company has notified the U.S. Food and Drug Administration under the Emergency Use Authorization (EUA) process.Arbor Vita'...

Read More