Health Insurance Portability and Accountability Act
US federal law protecting sensitive patient health information from being disclosed without consent.
Quick Facts
- Documents Included
- 37
- Category
- Healthcare & Life Sciences
- Regions
- United States
- Compliance Domains
- 5 domains
What's Included
SeedGovernance provides 37 ready-to-use templates for HIPAA, covering 5 compliance domains. Each document is pre-filled with framework-specific guidance so you can start immediately.
Privacy Rule
Policies, processes, and evidence templates
Security Rule
Policies, processes, and evidence templates
Breach Notification
Policies, processes, and evidence templates
Business Associates
Policies, processes, and evidence templates
PHI Safeguards
Policies, processes, and evidence templates
How SeedGovernance Helps with HIPAA
Beyond templates, our platform guides you through every step of HIPAA compliance.
Assessment Wizard
Answer guided questions to assess your HIPAA readiness and identify gaps.
Gap Analysis
Automatically surface what's missing from your HIPAA compliance programme.
Document Library
37 pre-built templates tailored to HIPAA requirements.
Operations Modules
Track incidents, changes, risks, and vendors — all mapped to HIPAA controls.
KPI Dashboard
Monitor your HIPAA compliance score in real time with automated metrics.
Auditor Access
Share a read-only view of your HIPAA compliance status with auditors.
Related Frameworks in Healthcare & Life Sciences
Organizations using HIPAA often also need these frameworks.
FDA
41 documents
FDA regulations on electronic records and signatures in pharmaceutical and medical device industries.
EU MDR
18 documents
EU regulation governing the production and distribution of medical devices in the European market.
MHRA
16 documents
UK Medicines and Healthcare products Regulatory Agency framework for medical devices and pharmaceuticals.
GxP
14 documents
Quality guidelines and regulations for life sciences covering GMP, GLP, GCP, and GDP.
ICH GCP
14 documents
International standard for the design, conduct, and reporting of clinical trials involving human subjects.
ISO 13485
14 documents
Quality management system standard for organizations involved in medical device lifecycle.
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