Close Menu
    Facebook X (Twitter) Instagram
    Facebook X (Twitter) Instagram
    Subscribe
    • Home
    • Top Stories
    • Business
    • Tech
    • Companies
    • Events
    • Announcements
    Home»BioTech»Joonghun Pharmaceutical of Korea Targets Overseas Markets for Coronavirus Diagnostic Kits
    BioTech

    Joonghun Pharmaceutical of Korea Targets Overseas Markets for Coronavirus Diagnostic Kits

    Marie JonesBy Marie JonesJune 9, 2020Updated:June 9, 2020No Comments3 Mins Read
    Share
    Facebook Twitter LinkedIn Pinterest Email

    With the worldwide spread of the Novel Coronavirus (COVID-19), orders for Korean diagnostic kits continue to roll in. As part of the effort to combat COVID-19, Joonghun Pharmaceutical announced that it was accelerating efforts to provide its JD COVID-19 qRT-PCR Kit for in vitro diagnostics internationally.

    The JD COVID-19 qRT-PCR Kit uses Real-time RT-PCR (Real-time Reverse Transcription-Polymerase Chain Reaction), currently the main testing method for detecting SARS-CoV-2 virus in COVID-19, because of its excellent sensitivity and specificity.

    Joonghun Pharmaceutical’s diagnostic qRT-PCR Kit targets a single gene (N gene) of the coronavirus, based on the FDA and CDC response to COVID-19. Targeting the single gene accords with FDA Test Validation FAQs which note recent evidence suggesting appropriately validated single gene detection (single viral target SARS-CoV-2 assay) provides acceptable performance. Joonghun’s targeting the N gene is based on the US CDC diagnostic kit ‘CDC 2019-Novel Coronavirus (2019-nCoV) Real-Time RT-PCR Diagnostic Panel’ which targets N genes as well.

    According to Joonghun Pharmaceutical, “We successfully conducted clinical trials using U.S. Food and Drug Administration (FDA) Emergency Use Authorization (EUA) clinical guidelines, in cooperation with university research institutes and government agencies.” Furthermore, “Based on these clinical results, on April 17 we obtained an export license from the Korean Ministry of Food and Drug Safety, and received a European in vitro diagnostic (CE-IVD) certification, providing us with a foothold for meeting various needs around the world.”

    Joonghun Pharmaceutical is currently attending results of its FDA EUA application, submitted May 4th, 2020. The FDA approval process is expected to proceed smoothly as the product was verified in clinical trials. A spokesperson for Joonghun Pharmaceutical said requests for the supply of diagnostic kits are constantly coming from South America, Europe and parts of Asia where COVID-19 is still spreading, and obtaining EUA approval would provide another source of validation for these markets.

    The company also produces the Joonghun Ribavirin capsule, one of 35 medicines recognized by the Korea Health Insurance Review and Assessment Service as a COVID-19 treatment. “Inquiries regarding Joonghun Ribavirin capsules surged from public institutions and distributors in countries across Europe and South America, and in March, at the request of Luxembourg, a total of 42,000 capsules were urgently exported.”

    “In order to contribute and help stabilize the global impact of COVID-19, we will increase the production of medicines, in order to respond quickly to urgent requests from domestic and international entities. Joonghun’s JD COVID-19 qRT-PCR Kit is produced in a GMP facility for pharmaceuticals and medical devices, so we will be able to provide a stable supply.” Joonghun Pharmaceutical also added, “In order to actively respond to the worldwide demand for diagnostic kits, we are also planning to release a rapid test kit in June.”

    Media contact
    Joonghun Pharmaceutical Co., Ltd.
    T: +82-2-2138-8114
    E: COVID-19TF@joonghun.com
    U: www.joonghun.com

    Joonghun Pharmaceutical Co
    Share. Facebook Twitter Pinterest LinkedIn Tumblr Telegram Email
    Previous ArticleEmerge 2020 HR Tech Summit
    Next Article US Donates P54.8m Supplies to Philippine Bureau of Fire Protection

    Related Posts

    ASN 2026: HighTide Therapeutics Presents New HTD1801 Data Highlighting Therapeutic Potential in Chronic Kidney Disease

    October 23, 2026

    Unicycive Therapeutics Announces FDA Acceptance of Oxylanthanum Carbonate NDA Resubmission and PDUFA Date of March 25, 2027

    October 22, 2026

    Micot Pharma Debuts MT200605 Huntington’s Disease Research in a Poster Presentation at MDS 2026 and Expands Development into Neurodegenerative Diseases

    October 12, 2026
    Add A Comment

    Comments are closed.

    Latest News

    • Formerra Adjusts Transportation Surcharge Amid Continued Freight and Logistics Pressures
    • Twin lighting fairs open with some 3,000 exhibitors showcasing global lighting solutions
    • 18th Hong Kong International Wine & Spirits Fair opens next week
    • Quant Group Validates Its Physical AI Foundation Model in a Working Restaurant Kitchen
    • Australian Made puts Singaporean approval centre-stage of its new campaign launch
    • Micot Pharma Showcases First-in-Class, Brain-Penetrant TrkB Agonist MT200605 at World Stroke Congress, Building the Case for Global Partnerships and Commercialization
    • Quant Group (02685.HK) Enters into Framework Procurement Agreement for Up to 2,000 Embodied-AI Robots Solutions – Physical AI Business Poised for Re-rating
    • Chervon names Joel Petersheim as Vice President, End User Research and Sales – OPE Commercial USA
    • Chervon Names Parker Wesley Clary Director of Field Sales – Southern Division
    • Chervon Names Maggie Jones Director of National Field Sales OPS
    © 2026 BusinessNewsAsia.com
    • About Us
    • Contact Us
    • BusinessNews.ph
    • AsiaPEVC.com
    • DevFiNews.com
    • RenewableEnergy.ph

    Type above and press Enter to search. Press Esc to cancel.