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Trinity Biotech plc (NASDAQ: TRIB) is an international leader in the diagnostics industry, focusing on the development, manufacturing, and marketing of clinical diagnostic products for both clinical laboratories and point-of-care settings. Headquartered in Ireland, Trinity Biotech has been at the forefront of the industry since its formation in 1992, employing over 350 people and offering more than 400 products to customers in 80 countries.
Through a blend of organic growth and strategic acquisitions, Trinity Biotech has built a comprehensive portfolio of diagnostic products. These include test kits for the detection of infectious diseases, sexually transmitted diseases, autoimmune and hemoglobin disorders, and tools for diabetes monitoring and control. The company also supplies raw materials to the life sciences industry, expanding its influence and reach within the global market.
Trinity Biotech's product lineup features well-known brands such as Recombigen, Unigold, MarBlot, Mardx, and Immublot. The company's operations are geographically segmented into the Americas and the rest of the world, with a significant portion of its revenue derived from the Americas.
Recent developments have seen Trinity Biotech making significant strides in the diabetes management sector. The company recently acquired biosensor technology from Waveform Technologies Inc., marking its entry into the wearable biosensor market. This new venture aims to develop a range of biosensor devices, starting with a continuous glucose monitoring (CGM) product. To lead this initiative, Trinity Biotech appointed Avinash Kale as the Continuous Glucose Monitor Programme Director. Mr. Kale brings extensive experience in MedTech R&D and will play a pivotal role in advancing the company's CGM technology.
The company's commitment to innovation and excellence is evident in its ongoing projects and partnerships. Trinity Biotech continues to expand its product offerings and improve existing technologies to meet the needs of healthcare providers and patients worldwide. The company's dedication to quality and sustainability ensures that its diagnostic solutions remain at the cutting edge of the industry.
Trinity Biotech's financial performance for the fiscal year 2023 has been robust, with the company reporting significant growth and key business updates. The company's strategic focus on diabetes management solutions and human diagnostics positions it well for future success and shareholder value creation. For more details, visit Trinity Biotech's website.
Trinity Biotech (Nasdaq: TRIB) reported a business update for Q2 2021, highlighting advancements in their product lines. The company is advancing its TrinScreen™ HIV product through the WHO approval process, expected to increase market share in Africa. They are also developing a SARS-CoV-2 antigen test and pursuing an EUA for their antibody test, although the FDA has deprioritized this application, limiting its market potential. Additionally, Trinity is expanding lab services in New York, enhancing its diagnostic offerings.
Trinity Biotech (TRIB) reported a 20.9% revenue increase for Q1 2021, totaling $25.6 million, compared to $21.2 million in Q1 2020. Point-of-Care revenues fell 43.4% to $1.9 million due to COVID-19 related delays in HIV test orders. Conversely, Clinical Laboratory revenues grew 32.9% to $23.7 million, driven by strong sales of COVID-19 products, particularly PCR Viral Transport Media. Gross profit rose 17.6% to $10.9 million, but gross margin decreased to 42.6%. Overall, the company shows resilience amid pandemic challenges with expectations for revenue recovery in the Point-of-Care segment.
Trinity Biotech (Nasdaq: TRIB) announces its Q1 fiscal year 2021 financial results will be reported on May 25, 2021. A conference call is scheduled for the same day at 11:00 am ET, where details will be discussed. Interested parties can access the call via various toll-free numbers, including 1-844-861-5499 for US callers. A replay will be available until June 1, 2021 with access codes provided. The company specializes in diagnostic products for both point-of-care and clinical laboratory markets, focusing on infectious disease detection.
Trinity Biotech has submitted its new HIV screening product, TrinScreen™ HIV, to the World Health Organisation (WHO) for approval. This product aims to enhance the company's existing HIV testing capabilities in Africa, building on its success with the Uni-Gold™ HIV test. The TrinScreen test detects HIV antibodies from a finger stick sample in under 12 minutes, boasting high assay sensitivity. A prior evaluation with 1,200 samples yielded excellent results. Approval from WHO is expected in months, during which the company will prepare for automated manufacturing in Ireland.
Trinity Biotech (TRIB) reported a 12.8% increase in fiscal year 2020 revenues to $102 million, up from $90.4 million in 2019. Point-of-care revenues decreased by 19.1% to $9.2 million, influenced by lower HIV sales and Covid-19 related logistical challenges. Conversely, clinical laboratory revenues surged 17.4% to $92.8 million, attributed to robust sales of Covid-19 products. The gross margin improved to 47.6%. Notably, the company achieved a profit after tax of $15.7 million, compared to a loss of $4.1 million in 2019, alongside a basic earnings per ADR of 75 cents.
Trinity Biotech (Nasdaq: TRIB) announced that it will report its financial results for the fourth quarter and fiscal year 2020 on March 25, 2021. A conference call will be held on the same day at 11:00 am ET to discuss these results. Interested parties can join the call via US Toll Free or International Toll numbers, and a webcast will also be available. The company specializes in developing diagnostic products for point-of-care and clinical laboratory markets, serving customers globally.
Trinity Biotech (Nasdaq: TRIB) has received CE Mark approval for its Covid-19 IgG ELISA antibody test, the Captia™ SARS-CoV-2 IgG ELISA. The test is now launched in the European Union and other CE Mark-recognizing countries following its introduction in the US under the FDA's Emergency Use Authorization. The test detects IgG antibodies and serves multiple purposes: confirming past infections, monitoring post-vaccination immune response, assisting in population immunity management, and pre-vaccination screening. The test shows 95.9% sensitivity and 100.0% specificity.
Trinity Biotech reported Q3 2020 revenues of $32.0 million, showing a 30.2% increase from Q3 2019. Point-of-Care revenues fell 46.8% to $2.1 million, impacted by COVID-19 logistics, while Clinical Laboratory sales rose 44.6% to $29.9 million. Operating profit surged to $9.1 million, a sevenfold increase, due to higher revenues and improved gross margins of 52.4%. The company launched a Covid-19 IgG ELISA antibody test, awaiting FDA approval, and anticipates ongoing strong demand for Covid-related products. Net profit stood at $7.3 million, with earnings per share at 35.0 cents.
Trinity Biotech (Nasdaq: TRIB) will report its third quarter 2020 financial results on November 17, 2020, followed by a conference call at 11:00 am ET. The call can be accessed via toll-free numbers in the US and internationally. A replay will be available until November 24, 2020. The company specializes in diagnostic systems, particularly for detecting infectious diseases and quantifying chemical parameters. Investors are advised that forward-looking statements involve risks, including regulatory impacts and competition.
Trinity Biotech (Nasdaq: TRIB) reported Q2 2020 revenues of $16.0 million, a 28.8% decline from $22.5 million in Q2 2019, primarily due to Covid-19's impact on its business. Point-of-Care revenues fell 41%, while Clinical Laboratory revenues dropped 27.5%. Gross profit increased to $6.9 million, achieving a gross margin of 42.9%. The company implemented cost-saving measures, resulting in a $0.5 million operating profit. Trinity Biotech is actively pursuing Covid-19 testing solutions, having filed for FDA approval for an ELISA antibody test.
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