About Us

Prevail InfoWorks is a global full service Clinical Research Organization (CRO) and Full Service Provider (FSP) with a unique combination of clinical operations expertise and the full suite of clinical systems.

Be ready to achieve the bet clinical outcomes in a shorter amount of time.

Request a walkthrough

Speak with our clinical experts to review how the Single Interface® can help sponsors and their teams conduct clinical trials.

← maybe later, take me back to home

Request a walkthrough

Speak with our clinical experts to review how the Single Interface® can help sponsors and their teams conduct clinical trials.

← maybe later, take me back
to home

Call us at +1 (267) 797-2001
or
request online:

With 15+ years of proven success in hundreds of Phase I-IV trials across virtually all indications, Prevail can help improve your trial outcomes with:

With Prevail’s Single Interface™ you are no longer in the dark

The Single Interface™ provides a complete and up-to-date picture of your studies for early observations, optimal decision and process support, and seamless vendor coordination. First, all of your clinical, diagnostic, logistical, and accounting data is automatically and continually integrated into the Central Repository. The data can be from your, our or your suppliers’ systems.

Waiting for information is a thing of the past

With all of your data now in one place, Prevail’s vast library of “out-of-the-box” and custom reporting, analytic and workflow tools leverage the aggregated data for actionable intelligence. This unlocks insights into every aspect of your study, from operational metrics tracking to visual patient profiles to safety and efficacy trends.

Identify problems sooner to improve quality, save money and maintain timelines

The Single Interface™ identifies sooner what is or is not going as planned, allowing you to verify your study assumptions and prevent quality problems, cost overruns and delays. When your newfound visibility uncovers issues, Prevail provides a 21st century toolbox to proactively manage outcomes and drive study success.

Everyone is aligned and equipped for study success

Easy and timely access to actionable intelligence allows everyone to perform at the highest level, coordinate efficiently, and avoid administrative waste. What took hours to do now takes minutes. Early observations of hidden trends, correlations and variableness in aggregate data and workflow processes equip everyone for study success. This cost-effective and turnkey solution can be implemented in four to six weeks.

With Prevail’s Single Interface™ you are no longer in the dark

The Single Interface™ provides a complete and up-to-date picture of your studies for early observations, optimal decision and process support, and seamless vendor coordination. First, all of your clinical, diagnostic, logistical, and accounting data is automatically and continually integrated into the Central Repository. The data can be from your, our or your suppliers’ systems.

Waiting for information is a thing of the past

With all of your data now in one place, Prevail’s vast library of “out-of-the-box” and custom reporting, analytic and workflow tools leverage the aggregated data for actionable intelligence. This unlocks insights into every aspect of your study, from operational metrics tracking to visual patient profiles to safety and efficacy trends.

Identify problems sooner to improve quality, save money and maintain timelines

The Single Interface™ identifies sooner what is or is not going as planned, allowing you to verify your study assumptions and prevent quality problems, cost overruns and delays. When your newfound visibility uncovers issues, Prevail provides a 21st century toolbox to proactively manage outcomes and drive study success.

Everyone is aligned and equipped for study success

Easy and timely access to actionable intelligence allows everyone to perform at the highest level, coordinate efficiently, and avoid administrative waste. What took hours to do now takes minutes. Early observations of hidden trends, correlations and variableness in aggregate data and workflow processes equip everyone for study success. This cost-effective and turnkey solution can be implemented in four to six weeks.

We were able to lock the database in less than one hour after receiving last patient data in a pivotal study of 227 patients at 45 sites, and the data quality was excellent.

--Small Us Biotech

We were up and running with integrated clinical, logistics, and financial oversight in 17 days for our large Phase III study, and enrolled the first patient on the 18th day.

--Mid-sized North American Pharmaceutical company

Prevail Expertise at Work

Prevail’s suite of integrated clinical, logistics and financial oversight systems were fully deployed in only 17 days in a large Phase III study, with the first patient enrolled on day 18.