Clinical development journey

Across a wide range of therapeutic areas, we develop regulatory strategies to help you most efficiently navigate complex processes and advance your program into the clinic and beyond.

Experts help shape a personalized solution, getting involved in the earliest stages of your project to understand and map requirements and develop a tailored strategy for your clinical program.

We improve patient recruitment and retention in your trial by thoroughly understanding patient pathways, determining optimal study site profiles and validating protocols that reduce patient and caregiver burdens.

Identify and enroll patients, prepare and train study sites to accelerate your development time and create the foundations for success.

You get a best-in-class solution for your study combining the latest technologies with knowledge and expertise to identify and resolve data discrepancies, identify trends, and ensure the highest data quality.

Monitoring and reporting your clinical data with a hands-on approach means you can make the right decisions at the right time in your project.

Expert analysis to inform decisions and help you maximize your trial data for any phase, in any therapeutic area, around the world.

Monitoring patient safety on an ongoing basis to ensure the progress of your clinical trials, minimizing protocol deviations and ensuring the highest possible data quality.

Managing adverse events and supporting the submission of expedited and periodic reports from clinical trial drug safety to post-marketing safety surveillance.

Sharing knowledge and experience in a wide range of global clinical research guidelines to tell your product’s story and help realize the full potential of your science.

Meeting regulatory standards and navigating through changing demands of studies while ensuring the integrity and safety of your trial to ICH GCP standards.

Proactively identifying, tracking and mitigating risk and using statistics to remove extraneous differences between sites and perform a holistic review for risk signals in integrated trial data.

Synthesizing data from different systems within your technology ecosystem to create a complete, near real-time view of your trial, generate insights, and inform your decisions, every step of the way.