Trusted by Research Teams

The PHI Redaction
Platform for
Medical Research

DocShield automates the identification and redaction of protected health information — so your research team can share data freely, stay PIPEDA-compliant, and protect patient privacy without slowing down discovery.

HIPAA
SOC 2 Type II
ISO 27001
PIPEDA
Zero Data Retention
18 PHI fields identified
99.7% accuracy
Clinical_Trial_Record_4782.pdf
Subject Name:████████████
Date of Birth:██/██/████
Subject ID:███-████-███
Site Address:████████████████████
Contact:███-███-████
Arm / Group:Treatment Arm B
Primary Endpoint:Reduction in HbA1c at 12 weeks

Certifications & Compliance Standards

PIPEDA
PHIPA / FIPPA
HIPAA
SOC 2 Type II
ISO 27001
50K+
Documents redacted
each month
99.7%
PHI detection
accuracy
<2s
Average document
processing time
18
HIPAA PHI identifiers
detected automatically

One platform built for
every compliance environment

Whether you need rapid deployment or complete data sovereignty, DocShield has a solution designed for your institution's requirements.

Cloud
DocShield Cloud
Built for research teams that need to start fast. Upload documents and receive redacted output in seconds — no infrastructure, no configuration.
Instant setup — no IT involvement required
AI detects all 18 HIPAA PHI identifiers automatically
Zero data retention — documents never stored on our servers
Full HIPAA audit trails with tamper-proof logging
REST API for integration with existing research pipelines
Self-Hosted
DocShield Self-Hosted
Built for regulated research environments. Deploy the full DocShield platform on your infrastructure with zero external connections.
Deploy on AWS, Azure, GCP, or on-premises bare metal
Air-gapped installation — zero external network dependencies
Full data sovereignty — your data never leaves your perimeter
Meets NIH Data Management & Sharing Policy requirements
Dedicated deployment support and white-glove onboarding

From identifiable to
de-identified in seconds

DocShield's AI pipeline handles the complexity of PHI detection — so your team can focus on research, not redaction.

Upload Documents

Submit patient records, clinical notes, or bulk research datasets via the browser or REST API. Supports PDF, DOCX, images, and scanned files.

AI Detects & Redacts

Our NLP model — trained on clinical text — scans every page, identifying all 18 HIPAA-defined PHI categories including indirect identifiers and date combinations.

Download & Audit

Download redacted documents instantly. Every redaction is logged with a tamper-proof audit trail — ready for IRB submission, sponsor review, or publication.

Built for every
research context

From Phase III trials to retrospective studies, DocShield handles the PHI challenge across the full spectrum of medical research.

Clinical Trials
Sponsor & IRB Data Submissions
Prepare de-identified case report forms and source documents for sponsor review, IRB submission, and regulatory filing — while maintaining a complete audit trail for GCP compliance.
Academic Research
NIH Data Sharing Compliance
Meet NIH Data Management & Sharing Policy requirements by publishing de-identified datasets to repositories. DocShield ensures your data release removes all identifiers under the Safe Harbor method.
Population Health
Large-Scale EHR De-identification
Process bulk EHR exports, claims data, or registry records at scale. DocShield's batch pipeline handles tens of thousands of records with consistent accuracy — ideal for epidemiological studies.
Retrospective Studies
Historical Record Analysis
Unlock decades of archived patient records for retrospective analysis. DocShield handles varied document formats and handwritten notes — making legacy data research-ready without manual effort.

Certified for the most
demanding standards

DocShield meets the privacy and security frameworks that govern health data in Canadian medical research — and supports cross-border work with US partners.

PIPEDA
PIPEDA
Canada's federal private-sector privacy law — governs how personal health information is collected, used, and disclosed by private research organizations
PHIPA / FIPPA
PHIPA / FIPPA
Ontario's Personal Health Information Protection Act and Freedom of Information & Protection of Privacy Act — applies to health information custodians and publicly funded research
HIPAA
HIPAA
US Health Insurance Portability and Accountability Act — required for cross-border clinical trials, US-funded studies, and collaborations with American research institutions
SOC 2
SOC 2 Type II
Independent third-party audit of DocShield's security, availability, and confidentiality controls — report available to your institution under NDA

Trusted by research teams
at leading institutions

"DocShield reduced our IRB submission prep time from two weeks to less than a day. What used to require a dedicated coordinator is now automated end-to-end."

Research Coordinator
Academic Medical Center, Phase III Oncology Trial

"We evaluated several redaction tools. DocShield was the only one that met our data governance bar while still being fast enough for our team to actually use in practice."

Data Governance Lead
Multi-site Hospital Research Network

"The self-hosted deployment was exactly what we needed for our federally-funded program. Our data never left our environment, and the audit trail satisfied our Program Officer."

Principal Investigator
NIH-Funded Population Health Study
30-Minute Live Demo

See DocShield
in action

We'll run a live document through the platform, walk through your compliance requirements, and help you find the right deployment for your research environment.

No commitment required · Response within one business day · Available for enterprise BAA