Bridget Ross Appointed New CEO at ChroniSense Medical

“We are pleased Bridget Ross will bring her talents to ChroniSense as CEO,” said Ilan Neugarten, Chairman of the Board of Rainbow Medical, ChroniSense Medical’s largest investor. “We are confident Bridget’s extensive and diverse leadership experience will deliver impactful healthcare solutions to patients and will drive ChroniSense to a leading position in the disease management space.”

Bridget Ross brings more than three decades of strategic, operational and leadership expertise. Prior to joining ChroniSense, she was President of the Global Medical Group at Henry Schein and a member of the company’s Executive Management Committee. There, she led the growth strategy for a $2.4B global medical distribution, solutions and services business, and delivered revenue growth double the industry average.  Before joining Henry Schein,

Bridget Ross served as Vice President, Commercial Operations, Johnson & Johnson (J&J) Medical Device Sector. In this role, she led a commercial operations integration for the ~$12B NA Medical Device business and was instrumental in driving operational efficiencies. Previously, Ms. Ross held multiple executive roles, including Global President at two J&J subsidiaries in the Women’s Health & Urology and Otolaryngology spaces, where she was responsible for the development pipeline and commercialization of multiple innovative products.

“I am delighted to join ChroniSense,” Ms. Bridget Ross said. “The company’s breakthrough technology has the potential to be transformative for patients – a true game-changer in the digital health segment. I’m excited and honored to join the dedicated team at ChroniSense to work toward bringing meaningful benefits to patients, caregivers and shareholders alike.”

“We are excited about the potential for our technology to have an even greater impact on the lives of patients, and we are looking forward to a successful journey with Bridget’s leadership,” said Danny Lange, Founder, President and Director ChroniSense Labs Israel.

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