Clinical trials are vital to the future of medicine and pharmaceuticals. Many of them are literally matters of life and death, studying the effect of potentially life-saving drugs or researching the impact of devastating diseases. So, why is it that the training of...
remote training and performance management
of virtual and hybrid clinical trial sites.
3 Steps for Reducing Costs and Errors in Clinical Trials
Clinical trial costs are trending upward, driven by a variety of factors, such as increasing trial complexity and rising travel costs for training, meetings and monitoring. While some of these factors are largely fixed, costs can be controlled by focusing on areas...
Embrace Innovation to Dodge Rising Trial Costs
The cost of conducting a clinical trial has been rising in recent years and that trend shows no signs of abating anytime soon. And that means that the clinical research industry needs to overcome its traditional resistance to change and adopt innovations that can save...
Selecting a Study-Specific Protocol Training Strategy
“The right tool for the right job” is a saying that applies in many situations across many industries. When it comes to clinical protocol training, research sites and sponsors need to determine what their ultimate goals are to correctly identify the best training...
Reducing Study Team Burden with Targeted Training
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.
Telling Ain’t Training
Whether ensuring GCP compliance or the correct application of a study protocol, training is a critical part of any clinical trial. During the life of a study, there may be several points at which a sponsor may require additional or more intensive training to...
Preventing Protocol Deviations With Simulation-Based Training
Protocol deviations can have a devastating impact on the quality and integrity of key study data and potentially affect patient safety. And there can be serious regulatory repercussions for failing to follow the protocol precisely, as well. Taking the right approach...
Enrolled Subject Training
Clinical trials are becoming increasingly patient-centric. Pro-ficiency has trained tens of thousand of patients in multiple therapeutic areas using it’s ground breaking Pro Patient online training system. Now Pro Patient is available for Enrolled Subject Training....
Make Your Studies More Proficient
Pro-ficiency Simulation Training Pro-ficiency is a simulation-based training platform and site-performance management system. Pro-ficiency mirrors site challenges through simulations of potential subjects to ensure sites are fully trained on the mission-critical...
Is Your Trial Training Compliant With FDA and ICH Regulations?
Are you outsourcing any of your protocol, GCP, or Safety training for investigations and site staff? Training is important for study quality and patient safety. There is no point in investing tens of millions in a clinical trial and not training the sites...