To ensure that we provide strategically aligned regulatory, clinical and pharmacovigilance operations services to our clients, we focus on three key areas. The first is the industry forces driving transformation in the life sciences. This includes listening to the voice of the patient, dedicating time to fully comprehend potential impacts of health authority guidances to our clients and being mindful of trends and insights throughout the competitive landscape. Our second key focus is to work with our clients to explore how embracing emerging technologies within drug development is impacting the human workforce, converting the human+ philosophy into intelligent, disruptive benefits. Our third focus is to keep working with pharma and biotech companies to create a better tomorrow together, today.
R&D services from pre-clinical to post-marketing
We combine our pharmacovigilance, regulatory and clinical operations talent within our global delivery centers, powered by intelligent technology solutions, to fulfill our client operational needs.
Ensuring identification, assessment, and recording of adverse effects is conducted through innovative, reliable technology and services.
Sharing our clients’ mission to bring medicines and therapies to patients faster, we strive to deliver end to end intelligent regulatory services. Learn more.
Clinical data services
Our integrated clinical services span all aspects of a standards-based lifecycle, from protocol concept through to submission.
How we work
Bringing a culture of innovation to our clients and encouraging positive disruption throughout the R&D process from pre-clinical discovery to post marketed lifecycle maintenance. Delivering patient centric capabilities through a life sciences industry lens. Being your partner of choice to deliver on your strategic portfolio and aspirations.