Automate GDPR and US privacy requirements, accelerate audits

Most privacy tools were built for enterprise software companies.
We built this for clinical and translational innovators.

• Pre-built DPIA + RoPA workflows
• Clinical-specific vendor management + audit logs
• Patient-data and regulated research alignment
• Ready-to-use templates and regulatory documentation
• SOC2-aligned architecture

Privacy requirements are expanding and regulators expect more rigor, not more spreadsheets.

Biotech teams don’t have:

• Time to manually maintain registers 
• Budget for enterprise compliance stacks 
• Headcount for dedicated privacy admins 
• Margin for audit errors in regulated environments
   

V2 solves that.

• DPIA Automation Auto-generate DPIAs with guided workflows and approval logging   
• RoPA Creation & Maintenance Maintain audit-ready processing records without spreadsheets   
• Data Subject Request Handling Transparent, documented DSR workflows to meet regulatory timeframes   
• Audit Logs & Governance Built-in traceability and exportable records for audit defense   
• Template Library Everything from privacy notices to DPAs and SCCs  pre-structured for biotech   

• Emerging and growth-stage biotechs 
• Clinical research teams 
• Digital health and diagnostics companies 
• AI-enabled and real-world-data biotechs 
• Biopharma service partners with regulated data flows

Aligned with:

• GDPR 
• CCPA/CPRA 
• Clinical data governance norms 
• Research & health-data privacy standards 
• SOC2 readiness

We built this after two decades of supporting clinical trials, working with regulators, and operationalizing privacy in real study environments.

This isn't a generic privacy product.

It is:

• Developed by biotech operators 
• Crafted around trial and research workflows 
• Built with patient protection in mind 
• Designed for operational speed and audit readiness