INCREASE YOUR STATISTICAL POWER WITH QUALITY RESULTS
We offer integrated solutions and services designed to ensure patient safety and measure the effectiveness of your study compound, including: ERT eCOA, Respiratory, Cardiac Safety and Imaging.
No more struggling with manual, paper-based systems that are prone to error and compromise data quality.
Easily add countries, languages and import/export requirements to your trials.
Get strategic insight into changing regulatory requirements and guidance.
LET OUR EXPERIENCE MINIMIZE RISK & COMPLEXITY IN YOUR TRIAL
With nearly 50 years of clinical and therapeutic experience, we balance knowledge of what works with a vision for what’s next so we can adapt without compromising standards.
GOODBYE UNCERTAINTY. HELLO CONFIDENCE.
We leverage decades of experience collecting and analyzing clinical efficacy and safety endpoints, technology leadership and regulatory expertise to minimize risk and data uncertainty so you can move ahead quickly.
Accelerate your research with electronic clinical outcome assessment (eCOA) technology that doesn’t get in the way. Our eCOA technology is simple and predictable with an intuitive environment that collects the same data from any mobile device, any study, anywhere.
Demand data quality and breathe easy in your respiratory trials. Managing risk and generating high quality data is notably difficult in respiratory trials. Complex protocols, lack of training and collection and analysis inconsistencies create uncertainty about a patient’s eligibility to participate in a trial, patient safety and a compound’s efficacy.
Monitor every heartbeat with precision and ensure safety. Cardiac safety is the number one reason promising drugs are halted in development or taken off the market. You need a clinical partner with the most experience and expertise to ensure safety and efficacy. We have more experience than anyone else – regardless of the trial phase or type.
Get results without the typical human bias with our advanced imaging technology. Imaging data is increasingly used in clinical trials – even as the primary endpoint for some. Minimize risk, get stronger science, reduced site burden, improve trial oversight and accelerate timelines with our purpose-built solutions that are tailored to key therapeutic areas.
REQUEST A MEETING OR DEMO TODAY
Our team of experts is always available to address any questions you may have about our integrated Safety & Efficacy solutions. Submit your contact information and we’ll be in touch shortly.