Turning Transitions Into Triumphs.
When your clinical trial faces unexpected challenges, we bring predictability, speed, and integrity — right when you need it most.
Predictability in Uncertainty
When your trial hits an expected challenge, we bring it back to predictability — with accountability, urgency and transparency.
Speed to Recovery
Whether you call it a rescue study or just need a little bit of extra help, we mobilize quickly to get stabilize and get your trial back on track.
Data Integrity, Preserved
We protect your data, your timeline, and your investment.
Transitioning with a committed CRO
A CRO transition can make or break your trial. A seamless handover enables quality, predictability, and minimal disruption.
When plans shift, we understand the pressure. That’s why our transition team brings proven experience to stabilize your study—safeguarding data integrity, timelines, and quality every step of the way. With global reach and deep regulatory knowledge, we restore predictability back into your clinical trial. From assessment to execution, we turn uncertainty into progress.
Helping sponsors, large and small, recover complex trials
Whether your study needs a rescue or just a little bit of extra help, Fortrea delivers stability and speed through decades of trial experience and a specialized transition committee—helping you regain momentum across any therapy area.
Augmenting your clinical trials
Augmenting your trial isn’t just extra help — it’s risk mitigation. When delays threaten timelines, adding experienced support can sustain continuity, accelerate progress, and safeguard quality.
Clinical trials are complex, and even the best teams face hurdles from slow site activation and staffing shortages to protocol deviations. In these critical moments, augmenting your trial with support from an experienced CRO ally can make the difference between delay and delivery. Our team integrates seamlessly to stabilize timelines, safeguard operations and reduce risk for insourced studies and outsourced trials.
Therapeutic Area and Global Proficiency
Scientific fluency accelerates onboarding and enhances trial quality. Global scale reduces your burden by having one trusted collaborator managing all regions and vendors.
Transitioning a study isn’t just about logistics — it’s about understanding the science behind your trial and having the global reach to operationalize it seamlessly. A CRO with deep proficiency in your therapeutic area can interpret data accurately, anticipate challenges, and engage effectively with investigators and regulators. Global scale matters too. You need an ally with “boots on the ground” in every country and region where your trial runs, maintaining compliance, speed, and continuity across borders.
