Solutions / Healthcare & Lifesciences
From provider networks to digital health, payer plans to clinical research, every interaction creates protected health information. Clarip helps healthcare organizations inventory PHI, honor patient rights, and operate confidently under a tightening web of state and global laws.
Trusted by leading providers, payers, and life-sciences innovators
The challenge
Patient data flows across EHRs, payer systems, patient portals, telehealth apps, and research platforms - each with different regulators watching.
EHRs, billing systems, patient portals, and telehealth apps all create siloed pools of PHI that are difficult to inventory and govern.
Right of access, amendment, and accounting of disclosures must be fulfilled within strict HIPAA timelines across every line of business.
Clinical trials, real-world evidence, and partnerships with life- sciences vendors require defensible de-identification and consent governance.
Recent OCR and FTC actions target tracking technologies on patient portals - making tag governance a regulatory necessity.
Capabilities
Clarip unifies consent, data discovery, subject rights, and risk intelligence — built for the regulatory and ethical weight of patient data.
Use Cases
From patient portal to clinical trial.
Govern consent for tracking, communications, and third-party integrations on every patient-facing surface.
Honor authorization preferences across plan websites, mobile apps, and member service centers.
Manage informed consent, withdrawal, and de-identification workflows across studies and life-sciences partners.
Run outreach and population-health programs with auditable authorizations and minimum-necessary controls.
Customer story
"Clarip gave us a single source of truth for PHI across our hospitals, clinics, and digital health products — and helped us close OCR-flagged tracking risks in under 60 days."
Chief Privacy Officer - National integrated health system
patient-portal tag remediation
hospitals unified on one platform
Regulatory coverage
Out-of-the-box workflows, disclosures, and reports for the regulations that govern patient data -maintained continuously by Clarip's privacy research team.
Quick answers to the questions privacy, legal, and engineering teams most often ask about Healthcare & Lifesciences.
Clarip's Automated Data Mapping continuously scans EHRs, claims systems, data lakes, and research environments to identify and classify PHI and other sensitive data classes. The live inventory supports HIPAA Security Rule risk analysis, minimum-necessary controls, and breach scoping with current — not annual — visibility.
Clarip's Universal Consent Management Platform centralizes HIPAA authorizations, marketing consents, and research consents across patient portals, mobile apps, connected devices, and call centers. Patients see and control one record; providers can prove the consent basis for every disclosure and AI use of their data.
Clarip's DSR fulfillment automates access, amendment, accounting-of-disclosures, and state-law deletion requests across clinical and non-clinical systems. Workflows respect HIPAA's exemptions while satisfying CCPA/CPRA, Washington My Health My Data, and similar state regimes that overlap with HIPAA at the edges.
Clarip inventories every AI model touching PHI, links it to lineage from the data map, and enforces purpose, consent, and minimum-necessary checks before training or inference. Documentation and monitoring align with HIPAA, FDA Good Machine Learning Practice, and EU AI Act high-risk obligations for clinical decision support.
Clarip controls and logs the PHI exposed to ambient scribes, copilots, and patient-facing assistants, enforces consent and purpose limits on retrieval sources, and produces audit trails for every prompt and output. Health systems can deploy generative AI without losing HIPAA accountability or patient trust.
Get a 30-minute walkthrough tailored to your EHR, patient portal, and digital health platforms-plus a custom risk assessment of your top patient-facing properties.