Business Wire

Mobidiag sai CE-IVD-merkinnän korona-, influenssa A-, influenssa B- ja RS-viruksen tunnistavalle Amplidiag® RESP-4 -testilleen

Jaa

Mobidiag Oy on saanut CE-IVD-merkinnän Amplidiag® RESP-4-molekyylidiagnostiikkatestilleen, jolla pystytään nopeasti tunnistamaan yhdellä kertaa yleisimmät hengitystieinfektioita aiheuttavat virukset SARS-CoV-2 (koronavirus), influenssa A, influenssa B ja RSV.

Kyseiset virukset aiheuttavat samankaltaisia oireita, joten lääkäreiden ei ole helppo päätellä, mikä virus potilaalla on. Amplidiag® RESP-4 -testillä virus pystytään määrittämään nopeasti ja luotettavasti yhdestä nenänielunäytteestä, mikä helpottaa oikean hoitopäätöksen tekemistä. Testi tehdään Mobidiagin Amplidiag® Easy -laitteistolla, jonka etuja ovat optimoitu näyteseulontaprosessi sekä automaattinen DNA/RNA:n eristys ja PCR-levyn valmistelu. Laitteisto perustuu vakiintuneeseen korkean suorituskyvyn PCR-tekniikkaan ja pystyy käsittelemään 46 näytettä noin kolmessa tunnissa.

Uusi testi laajentaa entisestään Mobidiagin diagnostiikkatestivalikoimaa.

Mobidiagin toimitusjohtaja Tuomas Tenkanen: ”Olemme erittäin tyytyväisiä saatuamme CE-merkinnän tavalliseen influenssakauteen ja Covid-19 epidemiaan liittyvälle Amplidiag® RESP-4 testillemme. Koska SARS-CoV-2 viruksen, influenssa A-, influenssa B- ja RS-virusten aiheuttamat oireet saattavat olla hyvin samankaltaiset, on erittäin tärkeää, että alan ammattilaiset pystyvät ne nopeasti erottamaan toisistaan sekä aloittamaan asianmukaisen hoidon.

Pyrimme myös kaikin voimin ylläpitämään Amplidiag®-testiemme tuotannon korkean omavaraisuuden, jotta uuden Amplidiag® RESP-4 -testimme saatavuus pysyy hyvänä tulevina kuukausina ja siten omalta osaltaan estää koronaviruksen leviämistä.”

Lisäksi Mobidiag kehittää parhaillaan Novodiag® RESP-4 -molekyylidiagnostiikkatestiä, jossa hyödynnetään yhtiön omaa Novodiag®-järjestelmää SARS-CoV-2-, influenssa A-, influenssa B- ja RS-virusten nopeaan tunnistamiseen. Testi täydentää Amplidiag® RESP-4 -testiä ja mahdollistaa hengitystievirusten nopean tunnistamisen ja siten varhaiset hoitopäätökset, tehokkaat epidemiologiset ja tartuntatautien torjuntatoimet sekä potilaiden ripeän eristämisen. Potilaat saavat kaiken kaikkiaan parempaa ja tuloksellisempaa hoitoa.

Huomautus: Mobidiag-testejä ei ole tarkoitettu kotikäyttöön. Ne ovat saatavilla vain terveydenhuollon ammattilaisille. Noudata oman alueesi suosituksia ja toimintaohjeita, jos sinulla on hengitystieoireita.

Huomautuksia toimittajille

Tietoja Mobidiagista

Mobidiag on ripeästi kasvava molekyylidiagnostiikkayhtiö, jonka nopeat, kustannustehokkaat, luotettavat ja laajasti sovellettavat molekyylidiagnostiikkamenetelmät mahdollistavat patogeenien ja niiden mahdollisen antibioottiresistenssin nopean tunnistamisen ja siten tartuntatautien ja mikrobilääkeresistenssin (AMR) leviämisen ehkäisemisen. Mobidiag tarjoaa Amplidiag® ja Novodiag® -tuotteillaan kaikenkokoisille laboratorioille laajan valikoiman molekyylidiagnostiikan ratkaisuja tartuntatautien tunnistamiseen.

Mobidiagin pääkonttori sijaitsee Espoossa, ja sillä on tytäryhtiöt Ranskassa, Isossa-Britanniassa ja Ruotsissa. Lue lisää osoitteessa www.mobidiag.com

Contact information

Tilaukset ja tekniset kysymykset: sales@mobidiag.com

Mobidiag
Dorothee Allard, Marketing Communications Manager
+33 1 55 25 17 13
marketing@mobidiag.com

Consilium Strategic Communications
Chris Gardner, Matthew Neal, Melissa Gardiner
+44 (0)203 709 5700
mobidiag@consilium-comms.com

Tietoja julkaisijasta

For more than 50 years, Business Wire has been the global leader in press release distribution and regulatory disclosure.

Tilaa tiedotteet sähköpostiisi

Haluatko tietää asioista ensimmäisten joukossa? Kun tilaat mediatiedotteemme, saat ne sähköpostiisi välittömästi julkaisuhetkellä. Tilauksen voit halutessasi perua milloin tahansa.

Lue lisää julkaisijalta Business Wire

University of Siena Researchers Demonstrate Rapid UV Disinfection of Operating Rooms Between Surgeries14.4.2021 15:00:00 EEST | Press release

UltraViolet Devices, Inc. (UVDI), a global leader in Ultraviolet Air and Surface disinfection, announced new research demonstrating the UVDI-360 Room Sanitizer’s rapid disinfection of operating rooms between surgical procedures will be presented at the Society for Healthcare Epidemiology of America (SHEA) Spring Conference, taking place April 13-16, 2021. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20210414005184/en/ In the University of Siena research, the UVDI-360 Room Sanitizer effectively inactivated germs in operating rooms in six minutes. (Photo: Business Wire) In the research, conducted by Dr. Gabriele Messina, Professor of Public Health, University of Siena at the Rugani Hospital Monteriggioni in Siena, the UVDI-360 Room Sanitizer achieved a greater than 97% germ reduction in operating rooms in only six minutes, with two three-minute disinfection cycles run on each side of the operating table. Testing the UVDI-360 R

Amylyx Pharmaceuticals Provides Global Regulatory Update on AMX0035 for ALS14.4.2021 15:00:00 EEST | Press release

Amylyx Pharmaceuticals, Inc., a pharmaceutical company focused on developing new treatments for amyotrophic lateral sclerosis (ALS), Alzheimer’s Disease and other neurodegenerative diseases, today provided an update on its plans to advance AMX0035 through the clinical development process for the treatment of ALS. The company intends to submit a Marketing Authorization Application (MAA) for AMX0035 to the European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) by the end of 2021. As previously reported, the company plans to submit a marketing application with Health Canada Q2 2021. The FDA has expressed an interest in seeing data from an additional placebo-controlled clinical trial prior to receiving a New Drug Application (NDA), the vehicle through which a pharmaceutical sponsor formally proposes that the FDA approve an investigational product. To fulfill the FDA’s request and to continue to build upon the growing body of evidence supporting AMX0035 for

Noxopharm Files Septic Shock Treatment Patent for Veyonda®14.4.2021 15:00:00 EEST | Press release

Australian clinical-stage drug development company Noxopharm Limited (ASX:NOX) announced an international patent application aimed at protecting the use of experimental anti-cancer drug, Veyonda® (idronoxil), in blocking the development of septic shock associated with infections such as COVID-19 and influenza viruses. Overall, septic shock is believed responsible for an estimated 10 million global deaths per year, with an estimated three million additional deaths due to the current pandemic. So-called ‘long COVID’ symptoms (e.g., long-lasting fatigue, breathing problems, headaches), along with severe organ damage (e.g., limb amputation, diabetes, kidney, and heart failure) and death are all are outcomes associated with septic shock. Veyonda is being developed as an anti-cancer drug based on immunostimulation and anti-inflammation functions. Its anti-inflammatory action stems from blocking of a signalling pathway called STING that normally serves as trigger for an inflammatory response

HTL Biotechnology and Echelon Biosciences Inc. announce strategic partnership to advance biopolymer platform and hyaluronic acid research tools14.4.2021 13:00:00 EEST | Press release

HTL, the worldwide leader in biotechnology solutions using hyaluronic acid (HA) and other biopolymers, and Echelon Biosciences Inc., a U.S.-based global supplier of biochemical reagents, assays, and services to research and development laboratories, announced today their new distribution and product development partnership. The partnership will enable distribution of high-quality HA and glycosaminoglycan (GAG), and the co-development of novel GAG products. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20210414005119/en/ HTL's campus is located in Paris, France. HTL, the worldwide leader in biotechnology solutions using hyaluronic acid (HA) and other biopolymers, and Echelon Biosciences Inc., a U.S.-based global supplier of biochemical reagents, assays, and services to research and development laboratories, announced today their new distribution and product development partnership. The partnership will enable distribution of h

Eckert & Ziegler to Build cGMP Facility for Radiopharmaceutical Services in Berlin14.4.2021 12:59:00 EEST | Press release

Eckert & Ziegler is proud to announce that it is expanding its production site in Berlin, Germany, with a new production facility for the contract manufacturing of radiopharmaceuticals. This new cGMP clean room suite with a total area of around 270 m² will be a 21 CFR 211 compliant, radiopharmaceutical manufacturing facility dedicated to late stage investigational and commercial stage radiopharmaceuticals and be operational from the first quarter of 2022. Together with a new U.S. based cGMP facility, Eckert & Ziegler will be able to provide radiopharmaceutical development services to companies looking for Europe, US and worldwide contract manufacturing. “We have decided to make this investment to meet the growing global demand for radiopharmaceutical services in both imaging and therapy products. At the moment, a large number of radiopharmaceutical substances from international pharmaceutical companies are in advanced clinical trials, some of them for broad indications such as prostate

VertiGIS Acquires Facility Management Software Partner KMS14.4.2021 12:00:00 EEST | Press release

VertiGIS, a leading geographic information systems (GIS) solution provider and software developer, announced today the completed acquisition of longstanding development partner KMS Computer GmbH. KMS is an established and trusted computer-aided facility management (CAFM) software specialist based in Dresden, Germany. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20210414005039/en/ KMS by VertiGIS is an established and proven provider of computer-aided facility management (CAFM) software based in Dresden, Germany. KMS is known for its GEBman software and has been supporting municipalities, industrial, service and utility companies, among others, with their facility and document management requirements since 1990. The flexible, end-to-end solutions are based on the latest web technologies and are suitable for internal or mobile use. (Graphic: Business Wire) VertiGIS is backed by global, technology-based investment firm Battery

IDEMIA and INTERPOL Further Their Partnership to Supply Brand New Multi-Biometric System14.4.2021 11:24:00 EEST | Press release

Following the renewal of an existing contract, IDEMIA will deliver INTERPOL’s new identification system that will usher in enhanced capabilities such as higher matching accuracy and more user-friendly interfaces. Designed and scaled so that police officers in member states can carry out an unlimited number of searches and analysis at will, MBIS, IDEMIA’s latest technological biometric solution, will allow up to one million forensic analysis searches per day. This includes fingerprints, palm prints and faces, making it the top performing automated biometric identification system on the market. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20210414005324/en/ (Photo: Business Wire) These capabilities pave the way for introducing the application of biometrics to other sectors. In addition to police investigations, INTERPOL plans to enable its members to query their database from border control stations. This latest alliance furth

Uutishuoneessa voit lukea tiedotteitamme ja muuta julkaisemaamme materiaalia. Löydät sieltä niin yhteyshenkilöidemme tiedot kuin vapaasti julkaistavissa olevia kuvia ja videoita. Uutishuoneessa voit nähdä myös sosiaalisen median sisältöjä. Kaikki tiedotepalvelussa julkaistu materiaali on vapaasti median käytettävissä.

Tutustu uutishuoneeseemme