With automated processes, centralized reporting, a safety letter feature, document exchange and storage, and consistent training experiences, Trifecta’s solutions expand the team’s capacity to focus on the study.
I think it’s just as effective as an investigator meeting.” – Study team member
You’re accustomed to the tediousness of sifting through emails and storing documents in multiple places. But you don’t have to settle for inefficiency.
Within a single system, sponsors and sites can upload documents (staff credentials, patient consent forms, and safety letters), track signatures, and save communications. The online system generates training certifications and serves as a document repository for sponsors and CROs to track, distribute, and manage materials across sites—whether for site start-up activities or training — to ensure total compliance. Explore our robust reporting features.
With Trifecta’s training solutions and translation capabilities, everyone–in every location around the globe–has access to the same high-quality information.
The ability to modify training for use across multiple studies and to exempt people from training saves significant time during a clinical trial.
Let’s say you need to train investigators for a new study due to a slight formulation change in a drug. If an investigator already completed Study A’s non-protocol specific documentation, you can exempt him or her from that training for Study B— saving hours of training time. In addition, Trifecta can adapt and re-use existing training to fit the new study and have it ready to use within a few days.
By offering non-protocol specific training online prior to a live meeting, you can decrease the in-person meeting time. This frees the team to focus the meeting on Q&A and deep interaction regarding protocol-specific information.
Let us show you how our easy-to-use solutions can work within your study or organization.Contact Trifecta