Scarritt Group and Pro-ficiency have combined forces to create a comprehensive solution for initiating new clinical trial sites called Virtual-SIV™.

Over 6,200 clinical trial sites have been remotely initiated using Virtual-SIV™. This solution combines the best of Pro-ficiency’s web-based, simulation-enabled clinical trial training solution, and Scarritt Group’s modern, remote-SIV solution.

Now, you can both train and conduct site-based activities remotely, using a seamless virtual platform that does not sacrifice PI engagement or quality.

6,200
VIRTUAL SIVs SUPPORTED
2,200
VIRTUAL IMs
CONDUCTED
12,000
SITE STAFF TRAINED VIRTUALLY
8,025
TOTAL IMs CONDUCTED
145
PHASE 2 AND 3 STUDIES LAUNCHED

With Virtual-SIV™, all sites are thoroughly trained before SIV, using Pro-ficiency’s Virtual Study Trainer. This web-based system uses adaptive simulation training, to train investigators and site staff to the highest performance standards possible. The Pro-ficiency dashboard shows when every site completes their training and is ready for SIV in real-time. The system provides a scorecard of predictive analytics that shows every site's strengths and specific knowledge, as well as any skill gaps that require remediation. The data provides a roadmap for how to support each site based on their specific needs.

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Looking for a Virtual-SIV™ solution? By integrating Scarritt Group’s best-in-class virtual conference center or VCC and Pro-ficiency’s simulation-enabled virtual training, we have created a seamless, turnkey solution for starting and managing the performance of your clinical trials.

With Virtual-IM™ and Virtual-SIV™, you can remotely engage sites all over the world on complex protocols remotely in addition to fine-tuning their performance throughout the study.

The Virtual-SIV™ Dashboard shows every site’s readiness for study initiation as well as revealing individual knowledge and skills gaps that are being actively remediated through eMentoring™ via Virtual Study Start’s adaptive learning system. You can also manage all required compliance documents and communications, such as safety letters, from one portal.

Never delay a study due to training compliance gaps, and onboard new site staff automatically to ensure they receive proper training for the study.

Virtual IM™ is a turnkey solution. It provides the tools Sponsors need to train investigators, conduct highly-engaging virtual IMs, initiate sites remotely, and also manage their performance throughout the study.

Protocol
Development

Avoid amendments and manage them better when they do happen.

Deploy Simulation-enabled Study Training

With Virtual Study Start, your study training is deployed before your IM. The results of this study show the relative strengths and risks of all your PIs and site staff. Therefore, these predictive analytics help better direct the investigator's meeting to address the investigator’s specific needs and knowledge gaps.

Virtual-IM™

Through VCC, you conduct your virtual IM on the most feature-rich and study-tested virtual conferencing platform for clinical trials.

Virtual-SIV™

Provide the virtual face-to-face tools and the training and document compliance tools you need to SIV any site in the world without a hitch.

Ongoing
Support

Continually train new site staff on amendments and any regulated documents, safety letters, and project plan changes. We also manage secure, read-and-acknowledge communications between the study team and the sites.

Ask for a demonstration of Virtual-SIV™ today!
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