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QuidelOrtho Corporation (symbol: QDEL) is a prominent American manufacturer specializing in diagnostic healthcare products that are distributed globally. The company focuses on the development, manufacturing, and marketing of rapid diagnostic testing solutions, which are crucial for both clinicians and patients worldwide. QuidelOrtho’s product portfolio includes immunoassay and molecular testing, clinical chemistry, and transfusion medicine, providing comprehensive solutions that aid in critical medical decisions.
With a strong geographical presence in North America, EMEA (Europe, the Middle East, and Africa), China, and other countries, QuidelOrtho generates the majority of its revenue from North America. The corporation is committed to innovation and quality, continually striving to improve diagnostic accuracy and efficiency.
Recent achievements of QuidelOrtho Corporation include significant advancements in rapid diagnostic testing technologies that ensure faster and more accurate results. The company has also entered strategic partnerships and launched new products that enhance its market position and expand its global footprint.
For investors and stakeholders, QuidelOrtho’s solid financial performance and ongoing projects demonstrate its robust growth potential. The company’s latest updates, news releases, and financial reports reflect its dedication to driving progress in the healthcare diagnostics industry.
Latest News:
- SAN DIEGO--(BUSINESS WIRE)-- QuidelOrtho Corporation announces new strategic partnerships and product launches aiming to bolster its market presence.
Quidel Corporation (NASDAQ: QDEL) announced its ongoing commitment to monitor and detect COVID-19 variants, particularly the Omicron variant. CEO Douglas Bryant stated that their PCR assays can cover all known sequences of Omicron, ensuring detection through in silico analysis. The company is also ramping up its manufacturing capacity to produce 70 million tests monthly by year-end. These efforts aim to provide affordable testing solutions to communities.
Quidel Corporation (NASDAQ: QDEL) participated in the 33rd Annual Piper Sandler Healthcare Conference, discussing its business and financial developments. The virtual fireside chat's recording is accessible for 90 days via Quidel's website. With over 40 years in the medical device industry, Quidel has pioneered rapid diagnostic testing solutions for various diseases, including COVID-19. The company focuses on providing accurate and affordable testing globally, under trusted brands like Sofia® and QuickVue®.
Quidel Corporation (NASDAQ: QDEL) reported strong financial results for Q3 2021, with total revenues of $509.7 million, a 7% increase from Q3 2020. Sales of COVID-19 products rose to $402.6 million, while influenza product sales grew to $13.8 million. GAAP EPS was $5.08, down from $5.33 in 2020. The company resolved litigation with Beckman Coulter, expecting annual cash payments between $70 million and $75 million. Quidel secured a $500 million agreement with the U.S. government for COVID-19 tests, and received CE Mark for its Savanna platform.
Quidel Corporation (QDEL) has announced its sponsorship of the Distinguished Speaker Series by the Bay Area Lyme Foundation, aimed at enhancing public awareness and education about Lyme disease. The series features expert speakers discussing important topics related to Lyme disease. Quidel's Sofia® 2 Lyme FIA test offers rapid diagnostic results, providing vital information within 15 minutes. This initiative supports the rising number of Lyme disease cases expected to reach 476,000 in the U.S. by year-end, promoting easier diagnosis and treatment.
Quidel Corporation (NASDAQ: QDEL), a leader in rapid diagnostic testing, will announce its fiscal Q3 2021 financial results on
Quidel Corporation is hosting a free webinar titled "Pediatric Lyme Disease: An Epidemic Within a Pandemic!" on October 21. This event aims to raise awareness about Lyme disease's impact on children, who represent nearly 30% of the 476,000 annual U.S. cases. Medical expert Robert A. Dracker will discuss symptoms and testing, including the rapid Sofia® 2 Lyme FIA test, which provides results in 15 minutes. The webinar is tailored for pediatricians and healthcare professionals, emphasizing the necessity for vigilance against Lyme disease in children.
Quidel Corporation (NASDAQ: QDEL) announced preliminary third-quarter results for 2021, forecasting revenues between
Quidel Corporation (NASDAQ: QDEL) announces the launch of its QuickVue® At-Home OTC COVID-19 rapid antigen test, now available without a prescription at over 7,000 CVS Pharmacy locations and online. This move addresses the surge in demand for rapid testing amidst the ongoing COVID-19 pandemic, particularly due to the Delta variant. The test, allowing for self-administration with results in 10 minutes, shows a positive agreement rate of 83.5% with PCR tests. Quidel is on track to achieve a monthly production target of 70 million tests by year-end, highlighting its commitment to improve testing access.
Olivia Goodreau, founder of the LivLyme Foundation, will share her Lyme disease journey in a webinar on August 19. Sponsored by Quidel, the session emphasizes early testing and features the Sofia® 2 Lyme FIA, which delivers results in 15 minutes. Goodreau's foundation has funded research and provided 54 grants to help those affected by Lyme disease. The webinar aims to raise awareness with expected attendance from healthcare professionals and researchers. Quidel, a leader in diagnostic solutions, supports initiatives to improve healthcare quality globally.
Quidel Corporation (NASDAQ: QDEL) reported a 12% decline in total revenue for Q2 2021, falling to $176.6 million compared to $201.8 million in Q2 2020. COVID-19 product sales decreased to $83.4 million, down from $109.0 million, while influenza product sales plummeted to $1.6 million. GAAP EPS was $0.45, significantly lower than $1.55 in the prior year. Despite challenges, core business revenue grew 24% to $91.5 million, driven by strong performance in Cardiometabolic Immunoassays. The Sofia® SARS Antigen test received Emergency Use Authorization for screening, supporting potential growth.