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HIPAA & EMA-Compliant Healthcare Redaction

Safeguarding Protected Health Information (PHI) and Commercially Confidential Information (CCI) in medical records and clinical study reports.

Healthcare organizations, CROs, and pharmaceutical sponsors face stringent disclosure requirements from HIPAA, the FDA, and the European Medicines Agency (EMA Policy 0070 / Clinical Trial Regulation). Ensuring anonymization without losing scientific context requires specialized expertise.

Anonymization for Clinical Studies & Patient Records

Our team handles clinical trial documentation (CSRs, investigator brochures, case report forms) as well as hospital medical records, psychiatric evaluations, and insurance claims with total confidentiality.

18 HIPAA Safe Harbor Identifiers

Systematic identification and removal of all 18 standard HIPAA identifiers including biometric data, dates, and geographic tags.

Supplementing EHR Platforms

Seamless workflow supplementation for healthcare organizations using Verisma or internal release-of-information software.

Need Redaction Support for Your Organization?

Speak with an HRS specialist to discuss your file formats, volume, and turnaround timeline.

Get an Immediate Quote

Quick Contact

Have a rush filing deadline or compliance question?

Email: info@hillredact.com

Hours: Mon–Fri 9am–5pm EST

24-Hr Rush Turnaround Available

Woman-Owned & USA-Based

Nationally certified by WBENC. 100% of operations located in the United States for total compliance assurance.

WBENC Certified