CLINICAL REDACTION STUDIO
RedactIt Pro
Purpose-built for biopharma regulatory disclosure. Designed by transparency experts.
Redaction software built for the people who do the work.
RedactIt Pro is a life sciences redaction studio designed from the ground up for CSRs, protocols, SAPs, submission documents and the regulatory disclosure workflows your redaction specialists already know.
The problem. A single submission package and even individual study documents can be thousands of pages long, and sponsors are publishing more documents like it every year. Redaction specialists spend many hours on repetitive redaction work. Generic tools and general-purpose AI were not built for regulatory clinical documents, they require training and workarounds, while legacy redaction solutions incorporate costly anonymization capabilities that sponsors don’t need.
BUILT FOR CLINICAL DOCUMENTS
Lives in Adobe Acrobat. 90+ clinical rule sets
No new environment to learn. No major IT implementation. Proprietary rule sets trained on clinical trial document structures for PPD and CCI — with two operating modes: Preconfigured for speed, Tuned & Configured for precision.
OFFLOADS THE HEAVY LIFTING
Automates detection. Preserves judgment
Auto-Tune optimizes proprietary rules across multiple passes. The redaction specialist focuses on items that require judgment, not repetitive detection work. Every decision is auditable, and every output includes the supporting documents.
BUILT BY
People who know transparency and regulatory disclosure
RedactIt Pro was designed by a team with decades of combined experience in clinical trial transparency, enterprise software development and AI, with direct input from redaction specialists who have redacted documents like yours.
BUILT FOR
Biopharma regulatory disclosure. Nothing else
Unlike general business redaction tools adapted to pharma, every rule set, every workflow step, and every audit artifact in RedactIt Pro was designed from the ground up for clinical documents. No need to train your vendor or compromise on capabilities.
90+
Proprietary rule sets
Trained on clinical trial document structures for PPD and CCI.
2
Operating modes
Preconfigured for speed. Tuned & configured for precision.
1
Redaction report
A summary report of redactions — a defensible audit trail for regulators and sponsors, PPD and CCI.
Ready to see it work on your documents?
Thomas Wicks · thomas@jakitollc.com — Early adopter pricing available through September 30, 2026.
RedactIt Pro 