Increase Efficiency and Accuracy of Audit Evidence for HIPAA, FDA/524B, ISO, HITRUST and EU/MDR
The ChronoProof GRC Platform is specifically designed for HIPAA, FDA Section 524B, ISO 14971 and the EU MDR device regulation. We can have you operationally testing in your environment within a week
Bring Your Own Cloud (BYOC) Hybrid Architecture
ChronoProof is installed on your system with the functionality necessary to meet point-in-time evidential audit requirements for Certification as well as managing Policies and Procedures, Risk Identification with Monte-Carlo Analysis and a Governance front end that is easy to modify as company reporting and analysis requirements expand.
Cost Optimization Structure
The BYOC hybrid model creates an optimal cost structure where development and testing costs remain with ChronoProof, while runtime costs are borne by your organization, who directly benefits from the application.
Data Sovereignty
Your data never leaves your Cloud controlled environment
Compliance Alignment
Supports FDA, ISO, HIPAA & HITRUST regulatory requirements
Security Control
Customers maintain full security oversight and management
Integration Flexibility
Seamless integration with your existing infrastructure
We support the installation of ChronoProof on your system
Capture evidence on a monthly or quarterly basis quickly, timely and accurately with minimal effort by your IT staff, which substantially reduces the audit evidence load once the audit begins.
Integrated Workflow Automation for evidence collection
Authentication
Policy and Procedure Development and Integration
Immutable Timestamping
Secure Storage
Third Party Risk Management Solution Set
Metadata Documentation
Audit Readiness Workflow
Complete Control and Flexibility to add additional Frameworks
Chain of Custody
Complete API integration with MyCSF
Complete GUI front end and SQL database control and development
See how ChronoProof can help.
Contact ChronoProof today to see how we can help reduce your GRC Platform is specifically designed for HIPAA, FDA Section 524B and the EU MDR device regulation. We can have you operationally testing in your environment within a week. Today.