CONSHOHOCKEN, PA — Suvoda LLC announced it has completed its brand integration with Greenphire, consolidating both companies ...

Sanofi and QuantHealth team up to advance AI-powered digital twins and clinical trial simulations to accelerate drug ...

Cecilia Bahit, MD, and Carolyn Lam, MBBS, PhD, FACC, discuss the barriers patients face when seeking access to clinical trial enrollment.

The gene therapy landscape has changed dramatically in the past 5 years, and investigators wanted to capture and analyze the details of current and upcoming trials, along with their potential impact ...

CONSHOHOCKEN, Pa., Sept. 25, 2025 /PRNewswire/ -- Suvoda LLC, a global clinical trial technology company, today announced the completion of its brand integration with Greenphire, unifying both ...

The U.S. Food and Drug Administration (FDA) has granted orphan drug designation to AMXT 1501 in combination with ...

The FDA's removal of draft guidance on clinical trial diversity raises concerns about its commitment to diversity and compliance with statutory obligations. The draft guidance aimed to improve the ...

Lizzy Lawrence leads STAT’s coverage of the Food and Drug Administration. She was previously a medical devices reporter. You can reach Lizzy on Signal at lizzylaw.53. An effort by the Trump ...

Clinical trials allow doctors and researchers to evaluate the effectiveness and safety of various medical treatments. A person with a greater chance of developing a specific condition who meets ...

Aria Trivedi is a biology major with a minor in biotechnology, and she is a 2024-25 health care ethics intern at the Markkula Center for Applied Ethics at Santa Clara University. Views are her own.