Changelog

What's new in Capture.Study

A running record of new and expanded capability across the platform — EDC, ePRO, eConsent, randomization, safety, and study oversight. Expand any entry for the detail; this isn't a full engineering log, just what actually changes how you run a study.

September 2026

August 2026

July 2026

See it running in a real study

Every capability above is live on the platform today. Book a walkthrough and we'll show you the parts most relevant to your protocol.

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What's new in Capture.Study

September 2026

A more detailed, more trustworthy audit trail

A formal workflow for correcting study data

A dedicated path for rescreening participants

Quality Tolerance Limits and a live risk register

A dedicated Reports section, plus richer data-review status

Stronger separation between blinded and unblinded roles

Electronic signatures extended to data lock and unlock

A Compliance Register, and deletions that leave a trail

Configurable lab reference ranges and clinical flagging

More PROMIS instruments, license tracking, and tablet-ready ePRO

Cleaner exports: source form, version, and readable answers

Site lifecycle tracking, and consent forms that can be approved

AI-assisted eCRF building, straight from a spreadsheet

Concomitant medications get their own record

August 2026

Randomization: spreadsheet import and blinded-safe exports

A complete workflow for data queries

Recurring ePRO diaries

Investigational product: shipments, dispensing, and destruction

A milestone-based visit schedule builder

July 2026

Calculated fields, with unit-aware conversions

MedDRA/CTCAE coding and investigator sign-off for adverse events

A formal unlock workflow, and support for partial dates

See it running in a real study