• built around clinical trial sites.

Improves clinical trial outcomes for
patients., clinical trial sites., sponsors.

By enabling clinical trial sites to do their best work, Concordare supports all stakeholders in the clinical trial process

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.

Learn more about how Concordare supports all stakeholders
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.

Pick a protocol

Select a protocol no matter what stage of the clinical trial life cycle

Use Concordare Suite to digitize

Convert your protocol to a digital CPTM using Concordare, or request a conversion

Distribute the CPTM

Share the CPTM with all key stakeholders, whether that be an internal study team at the site for investigator initiated trials or by sharing it with many sites for sponsored trials

Create high quality clin. ops. tools

Using the Concordare SuiteTM, any stakeholder can immediately download consent forms, protocol trackers, calenders and much more

  • 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
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