- It is time to move past the 300 page protocol
Concordare Trials is a digital health company revolutionizing clinical trial operations through its innovative Concordare Suite and Clinical Protocol Trial Management (CPTM) format. By transforming traditional clinical trial protocols into actionable, standardized digital tools, Concordare streamlines study workflows, reduces human error, and accelerates trial timelines. Designed to empower clinical sites of all sizes, Concordare ensures compliance, enhances operational efficiency, and improves data quality. With a mission to democratize access to clinical trials, Concordare is setting new benchmarks in the digital transformation of clinical research.
The Genesis of Concordare
Concordare operates a digital format for clinical trial protocols (CPTM) and e-CRC suite known as Concordare Suite. Our purpose is to seamlessly transform any clinical trial protocol into practical tools for the clinical setting, empowering study sites to efficiently comprehend and manage a clinical trial.
Concordare is for any study, any site. It has the capability to convert any study into a CPTM, while our operational tools are specifically crafted to augment existing clinical site workflows without the need for a complete overhaul. The Concordare Suite enables sites to quickly access pre-formatted templates, encompassing vital tools such as daily schedule-of-event trackers, patient calendars, and billing grids.
- Concordare Suite Solutions
Concordare is different from all clinical trial solutions. It was conceived wholly from a clinical operations perspective ensuring that all stakeholders' needs are met
Patients
Patients no longer have to walk away from a clinical trial visit unsure of what their journey ahead looks like. Concordare offers many templates for patient calendars, checklists, and trackers to make sure patients better understand their care.
Site Staff
Are you tired of sifting through a 400 page protocol to find just the right dose for a patient experiencing an SAE? Concordare puts the answers to these questions at your fingertips. You no longer have to spend hours of your time creating patient calendars and consent forms.
Protocol Authors
Whether you are a sponsor conducting a multi-site study, or an investigator at a single site, Concordare has developed the solution to turning your classic PDF protocol into a super-charged digital protocol for immediate operationalization and execution.
- Higher clinical trial volume capacity
Concordare supports all stakeholders
Concordare prioritizes effective clinical trial site operations. Patients, sponsors, and site staff benefit when sites are able to rapidly operate a clinical trial and reinforce the ability to meet a study’s specific requirement.
HOW our product works
Go from a paper PDF to a super-powered digital protocol in minutes
Concordare SuiteTM allows you to create and read a digital protocol.
- WHY Concordare?
The perfect platform for clinical trials
- Versatile - Concordare converts any clinical tral protocol
- Effective - No gimmicky tech solutions, just immediate operational tools
- For all stakeholders - Concordare SuitsTM reads and writes your digital protocol