At Emmes Group, numbers tell a story of lasting impact. For nearly five decades, we’ve supported the world’s most complex clinical trials with scientific rigor, global reach, and cutting-edge technology. Our key metrics reflect not only the scale of our operations, but also the trust placed in us by leading sponsors, government agencies, and researchers around the world. These numbers are more than stats—they represent our commitment to uncovering the truth behind medical innovation.

The Veridix Biostats and Analysis Agent empowers biostatistics teams to deliver faster, cleaner, and more consistent outputs across the trial lifecycle. By automating TFL shell creation, interim analyses, and final reports, the agent eliminates repetitive formatting and QC tasks, reduces handoffs between teams, and accelerates time to insight. Built for scale, it brings greater efficiency and control to everything from DSMB packages to CSR-ready outputs - without disrupting your existing workflows.

As your clinical trial and site management partner, we go to great lengths to support your sites and their patients.

We provide a variety of tools and support mechanisms to prepare for trial success. Our Clinical Trial Manager is responsible for ensuring sites are set up for success and fostering a relationship which starts at site feasibility and builds through activation, maintenance, and closure.

To deliver life-changing medical advancements, the clinical research you put into global drug development requires dedicated and detailed management of clinical trial safety risks and high quality of medical monitoring.

As your partner in enabling patient safety and managing enrolled patients safely through the duration of your study, we can provide a forward-thinking approach and a coherent safety data plan.

Then, biostatistics services collaborates with you and clinical tri

Join us where collaboration between scientists, clinicians, biostatisticians, data scientists, and IT experts is producing the highest quality results.

What can we do for you?

Agile and flexible, we work collaboratively with you to define, collect, manage and analyze the quality data that supports your product development and public health ambitions.

To deliver your goals, we invest in our people, technologies and clinical data management processes and we’ve built a culture where data management teams are empowered to make valuable contributions.

Strong biostatistical support is essential to the design and execution of efficient, high quality clinical trials. Our trained, qualified, and experienced biostatisticians can help take your clinical trial or observational study from concept all the way through final analysis and reporting.

Our Legacy. Our Future.

Founded by biostatisticians in 1977, we’ve always been statistics-driven. Today, we have more than 90 biostatisticians at Emmes spread across the globe.

Together, we can help you overcome the unique challenges medical device development presents.

Emmes can help you navigate the investigational new drug, device and biologics regulatory pathways toward a successful product launch.

We understand how drug and medical device regulations impact your product regulatory approval timelines.