Recent Posts

News, Investor
Sanford Health partners with Congenica to provide answers for undiagnosed rare disease patients
Posted 25th March 2021

Sanford Health partners with Congenica to provide answers for undiagnosed rare disease patients

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News
Congenica signs distribution agreement with AmpliTech in France
Posted 15th March 2021

Congenica signs distribution agreement with AmpliTech in France

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News , Investor
Congenica Appoints Kamraan Shariff as Chief Business Development Officer
Posted 1st March 2021

Congenica Appoints Kamraan Shariff as Chief Business Development Officer

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Blog , Patient Advocacy
Rare Disease Day 2021 - Live Blog
Posted 24th February 2021

Rare Disease Day 2021 - Live Blog

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News , Blog , Product
Achieving the highest diagnostic yield possible with phenotype-based prioritization of variants
Posted 24th February 2021

Achieving the highest diagnostic yield possible with phenotype-based prioritization of variants

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Blog , Patient Advocacy , Chapter 5
Why a diagnosis is so important for rare disease patients
Posted 22nd February 2021

Why a diagnosis is so important for rare disease patients

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News , Investor
David Atkins joins the National Genomics Board as BIA SME representative
Posted 18th February 2021

David Atkins joins the National Genomics Board as BIA SME representative

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News , Investor
Congenica Enters Cancer Collaboration with University of Glasgow Spinout Gabriel Precision Oncology
Posted 3rd February 2021

Congenica Enters Cancer Collaboration with University of Glasgow Spinout Gabriel Precision Oncology

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Webinar on Demand: Enabling Genomic Medicine
Posted 29th January 2021

Webinar on Demand: Enabling Genomic Medicine

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News
Congenica Contributes to Key Priority within UK Rare Disease Framework
Posted 27th January 2021

Congenica Contributes to Key Priority within UK Rare Disease Framework

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Webinar on Demand: The role of automated classification in clinical rare disease reporting
Posted 20th January 2021

Webinar on Demand: The role of automated classification in clinical rare disease reporting

Read More
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News , Investor
Sanford Health partners with Congenica to provide answers for undiagnosed rare disease patients
Posted 25th March 2021

Sanford Health partners with Congenica to provide answers for undiagnosed rare disease patients

Read More
News
Congenica signs distribution agreement with AmpliTech in France
Posted March Mar 15th 2021

Congenica signs distribution agreement with AmpliTech in France

Read More
News , Investor
Congenica Appoints Kamraan Shariff as Chief Business Development Officer
Posted March Mar 1st 2021

Congenica Appoints Kamraan Shariff as Chief Business Development Officer

Read More
Blog , Patient Advocacy
Rare Disease Day 2021 - Live Blog
Posted February Feb 24th 2021

Rare Disease Day 2021 - Live Blog

Read More
News , Blog , Product
Achieving the highest diagnostic yield possible with phenotype-based prioritization of variants
Posted February Feb 24th 2021

Achieving the highest diagnostic yield possible with phenotype-based prioritization of variants

Read More
Blog , Patient Advocacy , Chapter 5
Why a diagnosis is so important for rare disease patients
Posted February Feb 22nd 2021

Why a diagnosis is so important for rare disease patients

Read More
News , Investor
David Atkins joins the National Genomics Board as BIA SME representative
Posted February Feb 18th 2021

David Atkins joins the National Genomics Board as BIA SME representative

Read More
News , Investor
Congenica Enters Cancer Collaboration with University of Glasgow Spinout Gabriel Precision Oncology
Posted February Feb 3rd 2021

Congenica Enters Cancer Collaboration with University of Glasgow Spinout Gabriel Precision Oncology

Read More
Webinar on Demand: Enabling Genomic Medicine
Posted January Jan 29th 2021

Webinar on Demand: Enabling Genomic Medicine

Read More
News
Congenica Contributes to Key Priority within UK Rare Disease Framework
Posted January Jan 27th 2021

Congenica Contributes to Key Priority within UK Rare Disease Framework

Read More
Webinar on Demand: The role of automated classification in clinical rare disease reporting
Posted January Jan 20th 2021

Webinar on Demand: The role of automated classification in clinical rare disease reporting

Read More
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Congenica is available as a CE Marked IVD clinical decision support platform for clinical diagnostic use for inherited genetic disorders in the UK and EU, Iceland, Lichtenstein, Norway, Switzerland and Turkey. In all other countries, ensuring compliance with relevant local, national and international clinical laboratory regulations is the responsibility of the laboratory.