•   DK

    • Få bedre odds

    Øg IVF-succesraten for din fertilitetsklinik

    En verden

    af genetiske løsninger

    Screening

    Jeg vil gerne være donor

    GENETISKE LØSNINGER FOR FAGPERSONER

    Amplexa Genetics tilbyder banebrydende tests, der hjælper fagfolk med at diagnosticere og vælge den rigtige behandling til deres patienter.

    COVID-19 LØSNINGER

    Uanset om det er dig selv, dine medarbejdere eller dine kunder, der skal testes:
    Amplexa Genetics har løsningen.

    FERTILITET

    Amplexa Genetics tilbyder: test af befrugtede æg dyrket i forbindelse med IVF-behandling; test af kommende forældre for bærerstatus af sjældne arvelige sygdomme; kompatibilitetstest (klient-donor) og donorscreeningstest.

    TEKNISKE LØSNINGER

    Vi har forskellige omfattende, teknologiske løsninger, der kombinerer videnskab og informationsteknologi med vores bioinformatikservice, som kan tilpasses til ethvert område.

    VI KAN HJÆLPE DIG PÅ DIN FERTILITETSREJSE

    Når det kommer til fertilitetsproblemer, er behovene forskellige, og behandlingen varierer fra person til person.
    Vælg den Amplexa-test, som du mener svarer til din situation. Det kan du gøre ved at læse beskrivelserne nedenfor.

    Jeg vil gerne have et barn, men har flere mislykkede fertilitetsforsøg (IVF) bag mig.

    Anbefalet test:

    NON-INVASIV PGT-A

    Vi vil gerne være forældre, men inden da vil vi gerne vide, om vores barn kan arve en sjælden sygdom.
    Anbefalet test:

    GENES2LIFE

    Jeg vil gerne have et barn med hjælp fra en donor. Jeg er single.

    Anbefalet test:

    GENES4LIFE

    Uanset hvilken type familie du ønsker at danne, kan Amplexa Genetics hjælpe dig med at vælge en kvalificeret sæddonor.

    Anbefalet test:

    SÆDDONORSCREENING

    Uanset hvilken type familie du ønsker at danne, kan Amplexa Genetics hjælpe dig med at vælge en kvalificeret ægdonor.

    Anbefalet test:

    ÆGDONORSCREENING

    Jeg vil gerne være mor, men inden da vil jeg gerne vide, om jeg giver genetiske mutationer videre til mit kommende barn.

    Anbefalet test:

    X-LINKED CARRIER TEST

    Anbefalet test:

    GENES4LIFE PLUS


    NYHEDER

     Find us: Exhibit hall C3


     

    Meet us in Copenhagen!

    Amplexa Genetics will be participating as an exhibitor at ESHRE 2023. 

    European Society of Human Reproduction and Embryology (ESHRE)'s Annual Meeting is an international event that brings together reproductive medicine and science experts national event that brings together experts from the reproductive medicine and science field. It serves as a platform for scientific sessions, knowledge exchange, and invaluable networking opportunities among peers. 

    As a leading player in the field, Amplexa Genetics is honored to be a part of this esteemed gathering. We look forward to contributing to the vibrant discussions, sharing our expertise, and forging collaborations with fellow professionals. Our participation underscores our commitment to advancing research and education in reproductive medicine and embryology.  

    This event serves as a hub for presenting and discussing the latest developments and advancements, pushing the boundaries of reproductive medicine and embryology. 

    Amplexa Genetics is excited to showcase our innovative solutions, cutting-edge technologies, and research contributions during the ESHRE 2023 conference.

     

     

    Amplexa is Børsen Gazelle Regional Winner for Southern Denmark 2022

    It’s now official, and we’re bursting with pride: Amplexa is Børsen Gazelle Regional Winner for Southern Denmark 2022!
     
    We received the fantastic news on Thursday at the Regional Award Ceremony at Odense Odeon. We were dressed up in our best attire and had a blast of an evening, celebrating our new status with bubbles and tapas and selfies on the red carpet.

    Read more...

    PURPLE DAY, 26 MARCH

    Today, March 26th, is Purple Day, a day dedicated to raising epilepsy awareness worldwide. But at Amplexa, every day that we offer the best diagnosis in epilepsy is Purple Day.

    Epilepsy is among the most common chronic neurological diseases, with a prevalence of around 1% in the general population. 

    Read more...

    RARE DISEASE DAY

    Today, on Rare Disease Day, we get together to raise awareness of the challenges involved in living with a rare disease.

    At Amplexa we are passionate about raising community awareness through preventive actions. We make this possible with our gene panels: Genes2Life and Genes4Life.

    Read more...