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.

We know the unique challenges clinical studies of maternal and pediatric populations present.

We understand the physiological and ethical reasons for these challenges, and the diverse and discrete issues, and we are skilled in the nuances of this patient group. So our solutions in study design and implementation deliver high quality results acceptable to regulatory agencies and prominent journals.

Wherever health challenges arise, Emmes Group is there, advancing science, accelerating innovation, and making a difference worldwide.

At Emmes Group, we bring People, Science, and Technology together to deliver meaningful, measurable impact on global health.