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Validation Services with GoCompliance
GoCompliance’s validation pack and services are designed to reduce the time and cost of adhering to regulatory standards like ISO 13485, FDA 21 CFR Part 820 and Part 11 when deploying our compliance automation solutions.
Our validation service encompasses all 3 phases of process validation, from IQ (installation qualification) to OQ (operational qualification) to PQ (performance qualification).
We provide templates and supporting services to customize required documents for your specific configuration, execute test plans and/or generate final validation reports.
Feature / Capability | GoCompliance | Other Solutions | Agile PG&C | In-House Management |
|---|---|---|---|---|
Implementation & Onboarding Time | Deployment within weeks via GoSaaS implementation experts. | Variable — often multi-month projects. | Lengthy setup requiring internal IT and consultants. | Fully manual setup; no structured onboarding. |
User Experience / UI Design | Modern Redwood-style UI optimised for clarity and speed. | Generic web portal; not aligned with Oracle UX. | Legacy interface with slow navigation. | Manual files and spreadsheets; no UX standard. |
Data Centralisation & Analytics | Unified compliance hub with dashboards & exportable reports. | Pre-built reports only; limited customisation. | Requires IT to configure queries and dashboards. | Disconnected spreadsheets and files. |
DIY → Fully Managed Flexibility | Users choose level of automation and service based on need. | Multiple modules needed for scaling. | Rigid architecture; minimal configuration options. | Static manual processes. |
Supplier Collaboration Portal | Dedicated supplier portal for declarations, document uploads, and automated reminders. | Supplier modules available but often sold separately. | Supplier access possible but difficult to configure. | Manual email follow-ups and inconsistent tracking. |
AI-Powered Data Validation & Auditing | Agentic AI automatically flags missing, inaccurate, or risky supplier responses. | Rule-driven validation; AI limited or non-existent. | Manual rule-based checks. | Human-driven data review; no automation. |
Regulatory Monitoring & Automatic Updates | SiliconExpert integration provides real-time updates on 1 B+ parts and materials. | Updates provided quarterly or manually by support teams. | Requires manual list imports. | Users must track regulations independently. |
Pricing Model / Scalability | One fixed price with unlimited products, suppliers & specifications. | Tiered pricing; charges for suppliers and modules. | User-based licensing drives up cost as you scale. | Costs increase with labour and time commitment. |
Included Features
