Meridian Bioscience, Inc.  

3471 River Hills Drive
Cincinnati,  OH  45244

United States
https://www.meridianbioscience.com/
  • Booth: 2855

Meridian is a fully integrated life science company that develops, manufactures, markets, and distributes a broad range of innovative diagnostic products. We are dedicated to developing and delivering better solutions that give answers with speed, accuracy, and simplicity that are redefining the possibilities of life from discovery to diagnosis. Life Science Division - provides critical life science raw materials used in immunological and molecular tests for human, animal, plant, and environmental applications. Diagnostics Division - provides diagnostic solutions in areas including gastrointestinal and upper respiratory infections and blood lead level testing. We build relationships and provide solutions to hospitals, reference laboratories, research centers, veterinary testing centers, physician offices, diagnostics manufacturers, and biotech companies in more than 70 countries around the world.


 Press Releases

  • CINCINNATIJune 20, 2022 /PRNewswire/ -- Meridian Bioscience, Inc. (NASDAQ: VIVO), a leading global provider of diagnostic testing solutions and life science raw materials, announced today two new sample-specific master mixes, Lyo-Ready™ Direct DNA qPCR Stool Mix, and Lyo-Ready™ Direct RNA/DNA qPCR Stool Mix. These innovative master mixes improve the molecular detection of DNA and RNA from crude fecal specimens while allowing room temperature stabilization of diagnostic assays.

    Stool samples are used in many gastrointestinal diagnostic tests to screen for harmful bacteria, fungi, viruses, autoimmune conditions, and colorectal cancer (CRC). The fecal occult blood test (FOBT) has been the most widely used gastrointestinal immunoassay to screen CRC for over three decades. However, recent large-scale studies have shown that the FOBT lacks the sensitivity to detect early stages of CRC. Better diagnostic tools are needed to improve assay accuracy, sensitivity, and affordability. Molecular testing is the newest alternative and offers significant improvement in sensitivity and accuracy, especially when multiple targets are detected in the results of a multiplex test. Detection of DNA or RNA from stool is challenging because it contains an array of PCR inhibitors including bile salts, polysaccharides, and catabolic substances. To overcome these challenges, assays typically require expensive and time-consuming sample processing and extraction steps which increase the time to results and cost – ultimately delaying physician diagnosis and patient treatment.

    Meridian's new Lyo-Ready™ Direct DNA qPCR Stool and Lyo-Ready™ Direct RNA/DNA qPCR Stool Mixes remove the need for time-consuming nucleic acid extraction or lengthy component optimization. This enables test developers to quickly develop faster and more sensitive assays for stool sample analysis. In addition, the mixes can be used in liquid or lyophilized format when ambient temperature assay stabilization is needed, removing the need for cold storage.

    Florent Chang-Pi-Hin, Ph.D., Vice President of Research & Development - Life Science, commented, "The use of Lyo-Ready™ Direct qPCR Stool mixes for DNA and RNA is ideal for cancer biomarker detection, early cancer detection, and cancer treatment monitoring where assay sensitivity can be lifesaving. The specific adaptation of our chemistries to stool specimens makes our master mixes the perfect tool for any developer seeking faster new product introduction, shorter time to results, or the ability to transform a wet assay to an ambient temperature-stable assay with minimum developmental time."

    Meridian is committed to creating innovative solutions that simplify and accelerate the development of superior diagnostic assays. For more information on leveraging of Lyo-Ready™ technology for your assay development, please visit https://www.meridianbioscience.com/lifescience/products/molecular-reagents/lyo-ready-air-dryable-master-mixes-reagents/ or contact Paul.Marr@meridianlifescience.com.

    About Meridian Bioscience, Inc.
    Meridian is a fully integrated life science company that develops, manufactures, markets, and distributes a broad range of innovative diagnostic products. We are dedicated to developing and delivering better solutions that give answers with speed, accuracy, and simplicity that are redefining the possibilities of life from discovery to diagnosis. Through discovery and development, we provide critical life science raw materials used in immunological and molecular tests for human, animal, plant, and environmental applications. Through diagnosis, we provide diagnostic solutions in areas including gastrointestinal and upper respiratory infections and blood lead level testing. We build relationships and provide solutions to hospitals, reference laboratories, research centers, veterinary testing centers, physician offices, diagnostics manufacturers, and biotech companies in more than 70 countries around the world.

    Meridian's shares are traded on the NASDAQ Global Select Market, symbol VIVO. Meridian's website address is www.meridianbioscience.com.

    Contact:
    Charlie Wood
    Vice President – Investor Relations
    Meridian Bioscience, Inc.
    Phone: +1 513.271.3700
    Email: mbi@meridianbioscience.com

  • CINCINNATIMay 26, 2022 /PRNewswire/ -- Meridian Bioscience, Inc. (NASDAQ: VIVO), a leading global provider of diagnostic testing solutions and life science raw materials, announced today that its inhibitor-tolerant qPCR master mixes are ideal for the development of fast, accurate and highly sensitive qPCR monkeypox virus (monkeypox) molecular diagnostic tests.

    The recent outbreak of monkeypox has caused global concern due to its unprecedented rapid spread, resulting in what is feared to be the largest outbreak outside of Africa. Monkeypox is an orthopoxvirus first identified in monkeys and has historically only circulated in central and west Africa. Since May 13, 2022, more than 250 monkeypox cases have been reported to the World Health Organization (WHO) from 17 countries outside of Africa, with no known direct travel links to endemic areas.

    Screening assays that detect low levels of the virus will be instrumental in helping to contain the outbreak as it continues to spread globally.  Monkeypox has a long incubation period of up to three weeks, making traditional viral culture techniques not ideal for testing for monkeypox.  Serology testing is also challenging due to the close antigenic relation between surface antigens among the orthopoxviruses. Therefore, confirmation of monkeypox infection requires qPCR detection, which is considered the most rapid, sensitive, and accurate method for viral diagnosis.  Meridian has identified its inhibitor-tolerant qPCR master mixes as the best molecular master mixes in the portfolio for the detection of monkeypox.  These mixes have versions compatible with either wet or dry assay formats with its Lyo-ready™ (lyophilization ready) or Air-dryable™ technologies.

    "With any outbreak, it's critical to bring accurate testing to healthcare professionals as quickly as possible.  Meridian helped bring over 100 COVID-19 tests to market, including dozens in the early months of the pandemic, and is prepared to support diagnostic manufacturers in developing assays for monkeypox," commented Lourdes Weltzien, Ph.D. Executive Vice President - Life Science.  "Our inhibitor-tolerant qPCR mixes are perfect for developing monkeypox assays without the need for further optimization, greatly reducing development time.  Our team is standing by to help customers identify the best master mix for their application."

    Meridian continues to be steadfast in its commitment to bringing innovation and quality products to the IVD community, with a focus on developing tools that improve assay accuracy, increase operational efficiencies, and reduce overall costs to enable screening assays that are fast and affordable. To learn more about Meridian's innovative products, visit www.meridianlifescience.com/molecular-dx-reagents or contact Paul.Marr@meridianlifescience.com.

    About Meridian Bioscience, Inc.
    Meridian is a fully integrated life science company that develops, manufactures, markets, and distributes a broad range of innovative diagnostic products. We are dedicated to developing and delivering better solutions that give answers with speed, accuracy, and simplicity that are redefining the possibilities of life from discovery to diagnosis. Through discovery and development, we provide critical life science raw materials used in immunological and molecular tests for human, animal, plant, and environmental applications. Through diagnosis, we provide diagnostic solutions in areas including gastrointestinal and upper respiratory infections and blood lead level testing. We build relationships and provide solutions to hospitals, reference laboratories, research centers, veterinary testing centers, physician offices, diagnostics manufacturers, and biotech companies in more than 70 countries around the world.

    Meridian's shares are traded on the NASDAQ Global Select Market, symbol VIVO. Meridian's website address is www.meridianbioscience.com.

    Contact: 
    Charlie Wood
    Vice President – Investor Relations
    Meridian Bioscience, Inc.
    Phone: +1 513.271.3700
    Email: mbi@meridianbioscience.com

  • CINCINNATIMay 17, 2022 /PRNewswire/ -- Meridian Bioscience, Inc. (NASDAQ: VIVO), a leading global provider of diagnostic testing solutions and life science raw materials, announced today the continued expansion of its isothermal amplification product line with the launch of two new innovative master mixes, Lyo-Ready™ Direct DNA LAMP Saliva Mix and Lyo-Ready™ Direct RNA/DNA LAMP Saliva Mix. The usage of isothermal amplification, such as loop-mediated amplification (LAMP), is increasing globally. The most significant increases are seen in the point of care (POC) molecular diagnostics market and driven in part by the COVID-19 pandemic. The constant arrival of new COVID variants has resulted in a public demand for diagnostic assays that offer short sample-to-result time, high sensitivity, lower cost, and widespread accessibility.

    Lyo-Ready™ Direct DNA LAMP Saliva Mix and Lyo-Ready™ Direct RNA/DNA LAMP Saliva Mix are the first commercially available isothermal mixes designed explicitly for saliva and sputum samples and are compatible with lyophilization. Meridian's new master mixes combine the benefits of high inhibitor tolerance with fast isothermal amplification to enable ultra-sensitive detection directly from saliva or sputum. The mixes are uniquely designed for extraction-free amplification making them ideal for POC diagnostics. They are compatible with lyophilization to create ambient-temperature stable molecular diagnostic assays, providing significant cost savings and environmental benefits in shipment and storage.

    "Isothermal amplification methods such as LAMP are increasingly used in molecular diagnostics due to their compatibility with point-of-care devices and fast time to results. Our newest saliva-specific isothermal mixes are unique in the market and outperform other commercially available master mixes with faster time to results and significantly better amplification in terms of sensitivity and specificity. We are confident they will quickly become market-leading solutions for diagnostic assay developers," commented Lourdes Weltzien, Ph.D. Executive Vice President – Life Science. "Saliva is an important diagnostic specimen for a broad range of applications for detecting bacterial or viral infections, including respiratory infections such as COVID-19, and STDs such as HIV and herpes. Our new master mixes can help diagnostic companies develop high-performing assays efficiently with lower costs to the bottom line and the environment."

    Meridian is committed to supplying novel solutions to the diagnostic industry to simplify and accelerate the development of superior diagnostic assays. To learn more about Meridian's innovative reagents, visit https://www.meridianbioscience.com/lifescience/products/molecular-reagents/ or contact Paul.Marr@meridianlifescience.com.

    About Meridian Bioscience, Inc.
    Meridian is a fully integrated life science company that develops, manufactures, markets, and distributes a broad range of innovative diagnostic products. We are dedicated to developing and delivering better solutions that give answers with speed, accuracy, and simplicity that are redefining the possibilities of life from discovery to diagnosis. Through discovery and development, we provide critical life science raw materials used in immunological and molecular tests for human, animal, plant, and environmental applications. Through diagnosis, we provide diagnostic solutions in areas including gastrointestinal and upper respiratory infections and blood lead level testing. We build relationships and provide solutions to hospitals, reference laboratories, research centers, veterinary testing centers, physician offices, diagnostics manufacturers, and biotech companies in more than 70 countries around the world.

    Meridian's shares are traded on the NASDAQ Global Select Market, symbol VIVO. Meridian's website address is www.meridianbioscience.com.

    Contact:
    Charlie Wood
    Vice President – Investor Relations
    Meridian Bioscience, Inc.
    Phone:  +1 513.271.3700
    Email: mbi@meridianbioscience.com

  • CINCINNATIMarch 29, 2022 /PRNewswire/ -- Meridian Bioscience, Inc. (NASDAQ: VIVO), a leading global provider of diagnostic testing solutions and life science raw materials, announced today the launch of two new master mixes that detect DNA and RNA in crude blood samples down to a single copy – enabling the earliest detection of cancer using non-invasive liquid biopsy. These two innovative mixes, Lyo-Ready™ Direct DNA qPCR Blood Mix and Lyo-Ready™ Direct RNA/DNA qPCR Blood Mix, are designed for applications that require ultra-sensitive detection, such as liquid biopsy. This breakthrough technology is the first blood-specific, inhibitor-tolerant, and lyophilizable chemistry that enables extraction-free qPCR/RT-qPCR for liquid biopsy analysis at a performance level on par with traditional qPCR from purified nucleic acids.

    Liquid biopsy is a non-invasive alternative to tissue biopsy and offers ultra-sensitive detection of tumor-associated DNA or RNA from biofluids such as blood. Sample types like whole blood, serum, plasma, and the anticoagulants used for specimen stabilization contain PCR inhibitors that can significantly reduce detection sensitivity and may cause false-negative results. Inhibitors are usually removed by DNA/RNA extraction; however, that approach is very inefficient and increases assay time, cost, and the risk of contamination or error. Meridian's innovative Lyo-Ready™ Blood-Specific Master Mixes do not require extraction and are proven to excel with crude blood and its derivatives without the need to remove inhibitors. These groundbreaking mixes can help improve patient outcomes by enabling early cancer detection by delivering assay sensitivity down to one copy of DNA. Meridian's new mixes are formulated with lyophilization excipients, making them compatible with lyophilization to create room-temperature stable molecular diagnostic assays. Not only does this allow maximum sample input in the liquid biopsy analysis, but it also eliminates the need for cold chain storage of the finished test kit, limiting our customer's environmental impact.

    Florent Chang-Pi-Hin, Ph.D., Vice President, Global Research and Development, commented, "We are excited to expand our sample-specific molecular range with the market's first lyophilizable, and inhibitor-tolerant master mixes designed for direct amplification of nucleic acids from liquid biopsy. It is a truly disruptive technology that makes the early detection of cancer biomarkers directly from liquid biopsy a reality. We are proud of being the technology innovator enabling efficient and more cost-effective diagnostic assay development to help clinicians deliver the quickest, most accurate diagnosis for patients."

    Meridian is committed to supplying novel solutions to the diagnostic industry to simplify and accelerate the development of superior diagnostic assays. To learn more about Meridian's groundbreaking mixes, visit
    https://www.meridianbioscience.com/ambient-temperature-mixes or contact Paul.Marr@meridianlifescience.com.

    About Meridian Bioscience, Inc.
    Meridian is a fully integrated life science company that develops, manufactures, markets, and distributes a broad range of innovative diagnostic products. We are dedicated to developing and delivering better solutions that give answers with speed, accuracy, and simplicity that are redefining the possibilities of life from discovery to diagnosis. Through discovery and development, we provide critical life science raw materials used in immunological and molecular tests for human, animal, plant, and environmental applications. Through diagnosis, we provide diagnostic solutions in areas including gastrointestinal and upper respiratory infections and blood lead level testing. We build relationships and provide solutions to hospitals, reference laboratories, research centers, veterinary testing centers, physician offices, diagnostics manufacturers, and biotech companies in more than 70 countries worldwide.

    Meridian's shares are traded on the NASDAQ Global Select Market, symbol VIVO. Meridian's website address is www.meridianbioscience.com.

    Contact:
    Charlie Wood
    Vice President – Investor Relations
    Meridian Bioscience, Inc.
    Phone:  +1 513.271.3700
    Email: mbi@meridianbioscience.com

  • CINCINNATI and SEOUL, South KoreaJuly 7, 2022 /PRNewswire/ -- Meridian Bioscience, Inc. ("Meridian" or the "Company") (NASDAQ: VIVO), a leading global provider of diagnostic testing solutions and life science raw materials, and SD Biosensor, Inc. ("SDB") (KOSE: A137310) and SJL Partners LLC ("SJL") (collectively, the "Consortium") announced today that they have entered into a definitive merger agreement whereby a newly formed affiliate vehicle of the Consortium will acquire Meridian in an all-cash transaction valued at approximately $1.53 billion.

    Under the terms of the agreement, Meridian shareholders will receive $34.00 per share in cash, which represents a premium of approximately 32% over Meridian's closing stock price on the day before the Consortium's first offer before the market open on March 18, 2022 (closing price on March 17, 2022 was $25.67) and a premium of 16% based on the one-month average price per share of common stock commencing June 7, 2022.

    John C. McIlwraith, Meridian's Chairman, said, "This announcement follows an extensive and deliberate review of Meridian's growth and value creation opportunities in the context of the broader macroeconomic and industry environment. In consultation with external financial advisors and following outreach to potential strategic and financial partners, the Board unanimously agreed that this transaction represents the best path forward for Meridian shareholders, providing them with immediate, compelling and certain value, while enabling the Company to benefit from SDB's and SJL's capital support, expertise and experience."

    "We are excited to announce this new chapter for Meridian after the many years spent transforming the Company for sustainable growth," commented Jack Kenny, Meridian's Chief Executive Officer. "In addition to delivering immediate and significant value to our shareholders, we believe the transaction will enhance our ability to serve customers as we navigate the decline in COVID-19 testing demand and develop new products with the benefit of SDB's industry expertise and complementary offerings. Current and prospective employees around the world will also benefit from an even stronger Meridian supported by SDB's and SJL's financial backing and experience. I look forward to working with SDB and SJL and the rest of our Meridian team to build long-term strength and drive further growth in the diagnostics space."

    Dr. Young Shik Cho, Chairman of SDB, representing the Consortium said, "We are pleased to be a family with Meridian Bioscience as a great partner for accelerating our entry into the U.S. IVD market. I believe that SD Biosensor's R&D capabilities and mass production know-how, Meridian Bioscience's U.S. distribution network and expertise in the regulated U.S. market, and SJL Partners' strong management expertise will enable compelling synergies."

    Steve Sukjung Lim, Chairman and Managing Partner of SJL, said, "We are eager to begin this partnership with the Meridian team. The combination of Meridian's product commercialization team with deep expertise in the regulated U.S. market, SDB's broad product portfolio and scale manufacturing expertise, and SJL's execution experience and partnership model will further position the Company for long-term success."

    TRANSACTION DETAILS

    Completion of the transaction is not contingent on any financing condition. SDB, which is obligated to ensure that the Consortium funds the acquisition, will do so, together with SJL, through a combination of cash on hand and additional financing capacity, leveraging its strong balance sheet. Under the terms of the merger agreement, which has been unanimously approved by the boards of directors of Meridian and SDB, and the investment committee of SJL, the newly formed vehicle will acquire 100% of the outstanding shares of the Company. The transaction is subject to approval by Meridian shareholders, receipt of required regulatory approvals, the absence of specified materially adverse outcomes of Meridian's previously disclosed and ongoing investigation by the U.S. Department of Justice, and other customary closing conditions. The transaction is expected to close in the fourth calendar quarter of 2022. Upon completion of the transaction, it is expected that SDB will own approximately 60% and SJL will own approximately 40% of Meridian. Meridian will no longer be traded or listed on any public securities exchange.

    The Consortium intends to operate Meridian as an independent entity following the completion of the transaction and the Company's leadership team and headquarters are expected to remain in place.

    MERIDIAN THIRD QUARTER FISCAL 2022 RESULTS UPDATE

    This morning, Meridian separately announced preliminary results for the third quarter of fiscal 2022. Full financial results for the third quarter of fiscal 2022 will be released before the market opens on August 5, 2022. In light of the transaction with the Consortium, the Company will not host a conference call to discuss fiscal third quarter earnings.

    ADVISORS

    Rothschild & Co is serving as exclusive financial advisor and Jones Day and Keating Muething & Klekamp PLL are serving as legal counsel to Meridian.

    Piper Sandler & Co. is serving as exclusive financial advisor and Paul Hastings LLP is serving as legal counsel to the Consortium.

    FORWARD-LOOKING STATEMENTS

    This communication contains "forward-looking statements" within the meaning of the safe harbor provisions of the U.S. Private Securities Litigation Reform Act of 1995. Forward-looking statements can be identified by words like "may," "will," "likely," "should," "expect," "anticipate," "future," "plan," "believe," "intend," "goal," "seek," "estimate," "project," "continue," and variations of such words and similar expressions. Statements that are not historical facts are forward-looking statements. Forward-looking statements are based on current beliefs and assumptions that are subject to risks and uncertainties. Actual results could differ materially from those contained in any forward-looking statement as a result of various factors, including, without limitation: (1) economic or other conditions in the markets in which Meridian Bioscience, Inc. (the "Company") operates, including as a result of the COVID-19 pandemic or the Russia-Ukraine conflict; (2) the timing, receipt and terms and conditions of any required governmental and regulatory approvals of the proposed transaction that could reduce anticipated benefits or cause the parties to abandon the proposed transaction; (3) the occurrence of any event, change or other circumstances that could give rise to the termination of the merger agreement entered into pursuant to the proposed transaction; (4) the possibility that the Company's shareholders may not approve the proposed transaction; (5) the risk that the parties to the merger agreement may not be able to satisfy the conditions to the proposed transaction in a timely manner or at all; (6) risks related to distraction of the Company's management time from ongoing business operations due to the proposed transaction; (7) the risk that any announcements relating to the proposed transaction could have adverse effects on the market price of the Company's common stock; (8) the risk of any unexpected costs or expenses resulting from the proposed transaction or the delay thereof; (9) the risk that the outcome of any legal proceedings related to the transaction could be material to the Company or detrimental to the proposed transaction; (10) the risk that Company may be adversely affected by other economic, business, or competitive factors; and (11) the effect of the announcement of the transaction on the ability of the Company to retain and hire key personnel and maintain relationships with customers, suppliers and others with whom the Company does business, or on the Company's operating results and business generally. Should one or more of these risks or uncertainties materialize, or should underlying assumptions prove incorrect, actual results may vary materially from those indicated or anticipated by these forward-looking statements. Therefore, you should not rely on any of these forward-looking statements.

    Additional factors that may affect the future results of the Company are set forth in its filings with the Securities and Exchange Commission (the "SEC"), including the Company's most recently filed Annual Report on Form 10-K, subsequent Quarterly Reports on Form 10-Q, Current Reports on Form 8-K and other filings with the SEC, which are available on the Company's website at www.investor.meridianbioscience.com and the SEC's website at www.sec.gov, specifically under the heading "Risk Factors". The risks and uncertainties described above and in the Company's most recent Quarterly Report on Form 10-Q are not exclusive and further information concerning the Company and its businesses, including factors that potentially could materially affect its businesses, financial condition or operating results, may emerge from time to time. Readers are urged to consider these factors carefully in evaluating these forward-looking statements, and not to place undue reliance on any forward-looking statements. Readers should also carefully review the risk factors described in other documents that the Company files from time to time with the SEC. The forward-looking statements in these materials speak only as of the date of these materials. Except as required by law, the Company assumes no obligation to update or revise these forward-looking statements for any reason, even if new information becomes available in the future.

    ADDITIONAL INFORMATION AND WHERE TO FIND IT

    In connection with the proposed transaction, the Company intends to file relevant information with the SEC, including a proxy statement on Schedule 14A. This communication is not a substitute for the Proxy Statement or for any other document that the Company may file with the SEC and send to its shareholders in connection with the proposed transaction. Promptly after filing its definitive proxy statement with the SEC, the Company will mail the definitive proxy statement to each shareholder entitled to vote at the special meeting relating to the transaction. THE COMPANY'S SHAREHOLDERS ARE URGED TO CAREFULLY READ THE PROXY STATEMENT (INCLUDING ANY AMENDMENTS OR SUPPLEMENTS THERETO AND ANY DOCUMENTS INCORPORATED BY REFERENCE THEREIN) AND ANY OTHER RELEVANT DOCUMENTS IN CONNECTION WITH THE TRANSACTION THAT THE COMPANY WILL FILE WITH THE SEC WHEN THEY BECOME AVAILABLE BECAUSE THEY WILL CONTAIN IMPORTANT INFORMATION ABOUT THE TRANSACTION AND THE PARTIES TO THE TRANSACTION. The definitive proxy statement, the preliminary proxy statement, other relevant materials in connection with the transaction (when they become available) and any other documents filed by the Company with the SEC, may be obtained free of charge at the Company's website (www.investor.meridianbioscience.com) or the SEC's website (www.sec.gov). These documents may also be obtained free of charge from the Company by requesting them by mail at 3471 River Hills DriveCincinnati, OH 45244, Attention: Charlie Wood, Vice President – Investor Relations, or by email at mbi@meridianbioscience.com.

    PARTICIPANTS IN THE SOLICITATION

    The Company and its directors and executive officers may be deemed, under SEC rules, to be participants in the solicitation of proxies from the Company's shareholders in connection with the transaction. You may obtain information about the Company's executive officers and directors in the Company's definitive proxy statement for its 2022 annual meeting of shareholders, which was filed with the SEC on December 15, 2021. To the extent holdings of such participants in the Company's securities are not reported, or have changed since the amounts described in the proxy statement for the 2022 annual meeting of shareholders, such changes have been reflected on the Initial Statements of Beneficial Ownership on Form 3 or Statements of Change in Ownership on Form 4 filed with the SEC. These documents may be obtained free of charge at the Company's website (www.investor.meridianbioscience.com) or the SEC's website (www.sec.gov). Other information regarding the participants in the proxy solicitation and a description of their direct and indirect interests, by security holdings or otherwise, will be contained in the Proxy Statement and other relevant materials to be filed with the SEC in connection with the proposed transaction when they become available.

    About SJL Partners
    SJL is a Korea-based private equity investment manager uniquely focused on cross-border partnership investments with market-leading strategic companies to support their inorganic growth in international markets. SJL's portfolio includes investments into Momentive Performance Materials, a U.S.-based global leader in specialty silicones and silicone derivatives, Momentive Technologies, a leader in fused quartz and ceramic solutions, and Nexeon, a U.K.-based technology leader in anode materials for rechargeable batteries. Additional information is available at www.sjlpartners.com.

    About SD Biosensor, Inc.
    SD Biosensor, Inc., which is listed in KOSPI, is a global in-vitro diagnostics company that contributes to improving quality of life by diagnosing diseases quickly and accurately under the slogan 'Beginning of all things that protect lives.' SD Biosensor is a Total Solution Provider in the IVD industry, developing and researching innovative diagnostic platforms. From screening tests that general users can easily purchase and use oneself, such as BGMS and COVID-19 home test kit, to confirmatory tests that can check diseases qualitatively and quantitatively through medical staff like PCR, we have a diverse and comprehensive products portfolio. Our strengths are R&D capabilities, global sales network and mass production capacity. We are able to quickly develop new infectious diseases' products in many different platforms because of many experiences in the past in developing MERS, Ebola, and Zika antigen tests. Also, we provide many kinds of diagnostic products to 126 countries around the world through 517 designated dealers. SD Biosensor has WHO, ISO and KGMP approved top-tier production capacity in Korea. Additionally, we operate 3 factories in IndiaIndonesia and Brazil to increase cost effectiveness and prompt distribution. For further information, refer to our official website at https://www.sdbiosensor.com/.

    About Meridian Bioscience, Inc.
    Meridian is a fully integrated life science company that develops, manufactures, markets, and distributes a broad range of innovative diagnostic products. We are dedicated to developing and delivering better solutions that give answers with speed, accuracy, and simplicity that are redefining the possibilities of life from discovery to diagnosis. Through discovery and development, we provide critical life science raw materials used in immunological and molecular tests for human, animal, plant, and environmental applications. Through diagnosis, we provide diagnostic solutions in areas including gastrointestinal and upper respiratory infections and blood lead level testing. We build relationships and provide solutions to hospitals, reference laboratories, research centers, veterinary testing centers, physician offices, diagnostics manufacturers, and biotech companies in more than 70 countries around the world.

    Meridian's shares are traded on the NASDAQ Global Select Market, symbol VIVO. Meridian's website address is www.meridianbioscience.com.

    Investor Contact:
    Charlie Wood
    Vice President – Investor Relations
    Meridian Bioscience, Inc.
    Phone: +1 513.271.3700
    Email: mbi@meridianbioscience.com

    Media Contact:
    Bryan Locke / Monique Sidhom
    FGS Global
    Email: MeridianBioscience-FGS@sardverb.com


 Products

  • Curian® fluorescent immunoassay analyzer
    Curian® is a fluorescent immunoassay analyzer focused on gastrointestinal testing packaged in a small footprint. The standardized workflow provides sample to result in 3 easy steps with less than 1-minute hands-on time. Curian eliminates subjectivity while providing clean sample handling with Meridian’s all-in-one sample prep. Dual modes allow for flexible testing options to fit any workload....
       

  • Curian® is a fluorescent immunoassay analyzer focused on gastrointestinal testing packaged in a small footprint. The standardized workflow provides sample to result in 3 easy steps with less than 1-minute hands-on time. Curian eliminates subjectivity while providing clean sample handling with Meridian’s all-in-one sample prep. Dual modes allow for flexible testing options to fit any workload. Menu includes active infection H. pylori testing and Campylobacter antigen including C. jejuni, C. coli, C. upsaliensis, and C. lari species. Additional assays to follow include C. difficile GDH/Toxin and Shiga Toxin 1&2.
  • BreathID® urea breath test platforms
    The BreathID® urea breath platforms are designed to detect active infection H. pylori and confirm eradication. Eliminate workflow burdens with press and walkaway processing, features to reduce errors and streamlined reporting capabilities. BreathID is user-friendly and the most accurate non-invasive test on the market for H. pylori. Flexible testing options are available for any clinical setting....

  • The BreathID® urea breath test platforms are clinically recommended for initial active infection detection and confirmation of eradication for H. pylori. BreathID is an intuitive and patient-friendly solution with market-leading accuracy and efficient automation. The press and walkaway technology, flexible data management options and built-in error-reducing features provide optimal efficiencies to reduce workflow burdens. BreathID is the most accurate non-invasive test on the market for H. pylori. Three BreathID platforms are available for flexible testing options to accommodate any clinical setting. When it comes to H. pylori testing, Meridian is your trusted partner in gastrointestinal diagnostics. 
  • Revogene® Real-Time RT-PCR Molecular System
    Revogene® is a real-time RT-PCR platform with single analyte and multiplexing capability. The simplified sample prep in minutes, and ability to perform different assays simultaneously in the same run, provides flexibility to a laboratory’s workflow. The compact footprint, user-friendly interface, and bidirectional communication capability allows Revogene to integrate into any laboratory....

  • The time saving, walk-away efficiencies of Revogene® help laboratories deliver results through a flexible, standardized workflow with minimal steps. The simplified sample prep in minutes, coupled with the ability to perform different assays simultaneously in the same run, provides flexibility to a laboratory’s workflow. Revogene has an intuitive, user-friendly graphical interface, and its bidirectional communication capability can fully integrate the system into any laboratory. Using PCR technology with single analyte and multiplexing testing capability, Revogene delivers accurate results while meeting variable testing demands. The small instrument footprint allows the ability to be placed everywhere from the central laboratory to near-patient testing facilities. Revogene can be used in conjunction with Meridian’s rapid tests for a total solution that can enable healthcare systems to improve physician and patient satisfaction, standardize, and maximize operational efficiency.  

 Additional Info

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