Reimagining clinical trial operations

Clinical research coordinators spend the majority of their time on redundant manual work, copying the same trial specifications across source documents, EDC systems, and CTMS dashboards. Every system needs the same protocol requirements interpreted into a different format, and every update means rebuilding across every platform by hand.

Concordare is building the infrastructure to eliminate that redundancy. Our platform extracts trial information once into a structured Clinical Trial Protocol Model (CTPM) and generates every downstream deliverable automatically. One source of truth, used to run your entire operation.

con·cor·dare

[kon-kor-DARE]

verb, Latin

1.To agree; to be in harmony; to bring into accord.

Concordare exists to harmonize the people, protocols, and processes that drive clinical research forward.

Why we're building this

Clinical trials run on documents: protocols, eCRF guidelines, pharmacy manuals, and lab manuals. These are the backbone of every trial. For decades, these documents have been manually re-interpreted into every downstream system and tool a trial depends on, one study at a time, from static PDFs that can run 300 pages long.

Read the protocol. Extract the information. Build the trial. When an amendment drops, the cycle starts over. Across dozens of simultaneous studies, the redundancy compounds. It is not a people problem. It is a structural one, and it is exactly the kind of problem automation was built to solve.

We built Concordare to close that gap. Everything needed to generate the operational layer of a trial already lives in the study design documents. We made that extraction automatic. One digital protocol, every document and system integration that follows from it, built instantly, updated consistently, and reusable across every study on your roster.