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Pro-ficiency’s Commitment to Customer Service

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Good customer service starts with a great product. Without that…

Reducing Study Team Burden with Targeted Training

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Booming administrative tasks, customized technology systems and redundant certification and training requirements are among the primary factors that clinical research staff say eats up time better spent with patients and adds excessive burden—often uncompensated—to study teams. Tailoring training to both the protocol not only will better assure a sponsor that each employee at a site is getting exactly the training they need, but it will save research staff the time burden of going through training they don’t need.

Mitigating Study Risk With Performance Analytics

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Research sites are turning to various types of performance metrics to support risk-based management of clinical trials. “The first step in proactive data monitoring is to identify what is possible to mitigate, eliminate, and accept,” Hughes wrote. “This all forms part of various plans, including those for data, training, monitoring, statistical analysis, safety, medical monitoring, quality, and other functional plans.”

Correcting Site Enrollment In 3 Steps

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Patient enrollment is a common subject of discussion among both…

Reducing Protocol Deviations With Training-Based Metrics

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Protocol deviations can have a detrimental effect on new drug…

Telling Ain’t Training

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Whether ensuring GCP compliance or the correct application of…

SIVs: Identify Skill Gaps Before Retraining

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As a former CRA, I have spent the better part of my career mentoring,…

Preventing Protocol Deviations With Simulation-Based Training

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Protocol deviations can have a devastating impact on the quality…

Maximizing Site Enrollment with Improved Protocol Comprehension

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Sponsors and CROs trying to achieve better enrollment in clinical trials often overlook the most essential stakeholder in the process -- the investigative sites that implement the trials and interact with the patients throughout the process

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