The client is a global, publicly traded medical device manufacturer focused on developing new capabilities in near-patient diagnosis, monitoring, and health management. They had achieved significant growth through acquisition and needed a way to standardize the collection and management of clinical trial data enterprise-wide.
Month: July 2022
TIMELINE TO SUCCESS: EMERGENCY USE AUTHORIZATIONS march 2020 In fewer than 3 weeks, their client received emergency use authorization (EUA) from the FDA for its first point of care test. This was a valuable development due to its size (comparable to a small toaster) and…
This European company develops, produces and markets innovative devices for mechanically supporting the heart, and has developed a niche in pediatrics. Their products are known by cardiologists (where approved) to be highly reliable and engineered for utmost precision. With a solid position in the market,…
This global European company develops and markets synthetic bone repair materials for orthopedic and dental applications, and researches and develops bone graft technology. They develop, produce, and provide synthetic bone graft technology and highly sought after synthetic bone repair material, referred to as orthobiologics. They…