ClinOne Offers Complimentary Support to Researchers Racing to Develop the Coronavirus or COVID-19 Vaccine

The focal point of the initial outbreak was the Huanan Seafood Wholesale Market and the ingestion of common meals such as bat and snake; however, the zoonotic origin was quickly dispelled when more cases were identified outside of the market area and into other Chinese provinces, confirmation of person-to-person transmission, and utilization of medical imaging. To date, there are 79,360 confirmed cases worldwide, 2,619 associated deaths, and 24,963 cases that have recovered (Coronavirus COVID-19 Global Cases by Johns Hopkins CSSE, 23 February 2020).

The first confirmed death from COVID-19 occurred on 09 January 2020 and marked the beginning of the race to create a vaccine that will treat and prevent the ill effects of this coronavirus. Several pharmaceutical companies, the U.S. National Institute of Allergy and Infectious Diseases, Oslo-based Coalition for Epidemic Preparedness Innovations (CEPI), and a host of others have begun researching the cure; some are preparing for animal testing, and others are developing novel approaches to vaccine development. “Any vaccine will likely require human testing before final approval is awarded, and disease prevention can be achieved,” said Dr. Elizabeth Esterl, RN, VP of Operations and Research. “I am honored and humbled to offer the services of ClinOne to researchers worldwide. We are willing to assist in any way possible to stop the spread of this virus and associated deaths,” said Esterl, who has spent her career managing research institutions, including Colorado Children’s Hospital and National Jewish Health.

ClinOne offers the ability for researchers to connect directly to the patients, consent remotely, monitor symptoms of adverse reactions with wearable devices, and connect the sponsor, research sites and patients to ensure compliance and enhance the user experience. ClinOne is offering its support to accelerate the process of COVID-19 vaccine development to pharmaceutical companies by providing its clinical trial management technologies complimentary. “We are at an unprecedented time with managing the COVID-19 coronavirus outbreak around the world, and pharmaceutical partners are urgently needed to research and develop viable treatment options. We are here to support their efforts by providing the ClinOne suite of technologies free of charge,” said Rob Bohacs, CEO.

SourceClinOne

Hot this week

Cartessa Aesthetics Partners with Classys to Bring EVERESSE to the U.S. Market

Classys, which is listed on the KOSDAQ, is one of South Korea's most distinguished aesthetic technology manufacturers, with devices distributed in 80+ markets globally. This partnership marks Classys's official entry into the American marketplace, with Cartessa Aesthetics as the exclusive distributor for EVERESSE, launched under the Volnewmer brand in current global markets.

Stryker Launches Next-Generation of SurgiCount+

Now integrated with Stryker's Triton technology, SurgiCount+ addresses two key challenges: retained surgical sponges and blood loss assessment. Integrating these previously separate digital solutions provides the added benefit of a more efficient, streamlined workflow for hospitals notes Stryker.

Nevro Receives CE Mark In Europe for It’s HFX iQ™ Spinal Cord Stimulation System

Nevro notes HFX iQ is the first and only SCS system with artificial intelligence (AI) technology that combines high-frequency (10 kHz) therapy built on landmark evidence that uses ongoing cloud data insights to deliver personalized pain relief

Recor Medical Reports: CMS Grants Distinct TPT Device Code and Category to Recor Medical for Ultrasound Renal Denervation

The approval of TPT offers incremental reimbursement payments for outpatient procedures performed with ultrasound renal denervation for Medicare fee-for-service beneficiaries. It becomes effective January 1, 2025, and is expected to remain effective for up to three years notes Recor Medical.

Jupiter Endovascular Reports | 1st U.S. Patient Treated with Jupiter Shape-shifting Thrombectomy Device

“Navigation challenges during endovascular procedures are often underappreciated and have led to under-adoption of life-saving procedures, such as pulmonary embolectomy. We have purpose-built our Endoportal Control technology to solve these issues and make important endovascular procedures accessible to more clinicians and their patients who can benefit from them,” said Carl J. St. Bernard, Jupiter Endovascular CEO. “This first case in the U.S. could not have gone better, and appears to validate the safety and performance we are seeing in our currently-enrolling European SPIRARE I study.”
Exit mobile version