TransCure bioServices Strengthens team with C-suite hire and Boosts North American Preclinical Opportunities

A full-time CFO supports growth, while the new US-registered company grants locals end-to-end preclinical services access

TransCure bioServices, an AAALAC-accredited supplier of advanced humanized preclinical mouse models, is thrilled to announce the appointment of Céline Pinault as its new Chief Financial Officer. Pinault brings extensive experience in finance and business strategy, and her arrival marks a significant step in the company’s expansion. As part of this growth, TransCure bioServices has also registered a US company, increasing its reach in North America.

Céline Pinault joins TransCure bioServices with a robust background in financial management and strategic planning. Drawing on over 15 years of experience in finance leadership positions at well-established companies including AplusA, 5àsec and IPSOS, Pinault’s focus will be on driving the company’s global growth by acting as a specialist strategic finance officer.

“It’s an exciting time to join TransCure bioServices, as it continues to go from strength to strength,” says Pinault. “I look forward to helping the company deliver its ambitious global growth plans in a viable and sustainable manner. This will enable TransCure to help more customers bring novel therapeutics to market to overcome global healthcare challenges.”

As part of its growth plans, TransCure bioServices aims to provide all biotechnology and pharmaceutical companies the same wide range of technical services globally. While the CRO has been able to cater for North American customers from abroad, shipping and complex import regulations have caused challenges for both TransCure bioServices and its customers.

Now, the CRO has registered TransCure bioServices Inc. in the US to provide its North American customers with all the preclinical services offered in Europe. As a result, drug developers in the region get the same range of benefits in working with an end-to-end partner as their European counterparts, including the rapid delivery times they need to keep their studies on track.

“For safe and efficacious treatments to be brought to market quickly, it’s essential that researchers have access to high-quality preclinical services to support drug development,” says Kiave Ho Wang Yin, PhD, Chief Business and Innovation Officer at TransCure bioServices. “Between our existing sites, our new North American registration, and our recent Preclina partnership in the APAC region, we’re able to provide near-global support for organizations striving to advance healthcare.”

To learn more about TransCure bioServices’ offerings and leadership team, please click here: https://transcurebioservices.com/about-us/

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.”