The engine, that is the industry of clinical research, is one that has been built slowly, over many years, driven by the common human need for effective, affordable, and innovative healthcare. But, never was it tasked to a singular objective in the way it was when the world was struck by the COVID-19 Pandemic.

Data quality in clinical research is one of the most important aspects of a successful trial. This data is essential to the overall success of the clinical trial, not only from a regulatory standpoint, but as it highlights the effectiveness and safety of the drug or device being tested.

Acting as a repository for clinical operations, our CTMS includes functions for site feasibility and the tracking of action items and milestones. Throughout our platform, we deliver your clinical trial data across our products proactively in real-time, ensuring your team has the most up-to-date information to accelerate progress.

Real-world evidence (RWE) is data collected outside of traditional clinical trials, such as electronic health records (EHRs), claims data, patient-generated data, and social media data. RWE has the potential to transform clinical trials by providing a more comprehensive view of patient outcomes in real-world settings.

What we are seeing is a shift from the entirely patient-centric model, back towards sites. Hybrid trials, utilizing a combination of these strategies, are becoming more common and while our previous area of focus was on CROs, then patients, we are now hearing of an increased interest in solutions that target the needs of sites.

Ensuring that your trial goes live on time is essential for successful outcomes and bringing new treatments to market quickly and efficiently. In this blog, we’ll explore seven practical tips to help you stay on track and keep your trials running smoothly.