The latest article from Applied Clinical Trials addresses a key issue in drug development: how to close the gap between controlled clinical trial results and
This phase is vital for ensuring that all clinical aspects of the device are thoroughly evaluated and documented. 📋 Here are the key elements of
In our series showcasing BiTrial’s international presence, we highlight the dynamic research landscape and the key role Moldova plays in our global strategy. ✅EU candidate
Regulatory expertise for MD studies 🚀 ✅ Risk classification – We assess your device’s classification based on its intended use, technology, and patient impact, determining
In our series on the development lifecycle of medical devices, this time we take a closer look at the critical step of conducting preclinical studies.
The country is a hidden gem, often referred to as “Crna Gora” or “black mountain” by its inhabitants. As an EU candidate country and an
In this post, we take a closer look at early examples of medical records from before the James Lind era. At BiTrial, we’re passionate about
In our ongoing series, we’re diving deep into the crucial phases of medical device development. Today, we’re focusing on the device design and development phases,
The next country we’re introducing is Armenia. 🌍 This country offers numerous advantages we can successfully leverage in the field of clinical research. ✅👇 📅
At BiTrial, we believe the CEE region offers a unique combination of clinical potential, cost-efficiency, and patient engagement that makes it a smart choice for
