Armature
Armature provides a comprehensive quality management and compliance software platform designed to help you automate audits, manage certifications, and maintain high operational standards across your entire organization.
Greenlight Guru
Greenlight Guru provides a dedicated quality management platform designed specifically to help medical device companies navigate regulatory complexity and bring safe products to market faster.
Quick Comparison
| Feature | Armature | Greenlight Guru |
|---|---|---|
| Website | armaturecorp.com | greenlight.guru |
| Pricing Model | Custom | Custom |
| Starting Price | Custom Pricing | Custom Pricing |
| FREE Trial | ✘ No free trial | ✘ No free trial |
| Free Plan | ✘ No free plan | ✘ No free plan |
| Product Demo | ✓ Request demo here | ✓ Request demo here |
| Deployment | ||
| Integrations | ||
| Target Users | ||
| Target Industries | ||
| Customer Count | 0 | 0 |
| Founded Year | 2000 | 2013 |
| Headquarters | Newport, USA | Indianapolis, USA |
Overview
Armature
Armature is a flexible quality management platform that helps you move away from manual spreadsheets and paper-based tracking. You can manage the entire lifecycle of audits, inspections, and certifications within a single, secure environment. Whether you are overseeing a global supply chain or managing internal regulatory compliance, the software provides the tools you need to identify risks and ensure every department meets your specific quality benchmarks.
You can easily configure the system to match your existing workflows without needing extensive technical support. The platform allows you to schedule recurring audits, collect data in the field via mobile devices, and generate instant reports for stakeholders. By centralizing your compliance data, you reduce the risk of human error and ensure your organization stays ready for any external inspection or regulatory review.
Greenlight Guru
Greenlight Guru is a specialized quality management platform built exclusively for the medical device industry. You can move away from disconnected paper systems and generic tools to a centralized workspace that aligns with global regulatory standards like ISO 13485 and FDA 21 CFR Part 820. The platform helps you manage the entire product lifecycle, from initial design documentation to post-market surveillance, ensuring your compliance is always audit-ready.
You can accelerate your development timelines by using pre-validated workflows and automated traceability matrices. The software serves medical device startups, scale-ups, and established enterprises looking to reduce risk and improve product quality. By integrating risk management directly into your design process, you can focus more on innovation and less on administrative paperwork.
Overview
Armature Features
- Audit Management Schedule, conduct, and track audits from start to finish while maintaining a complete digital trail for every inspection.
- Mobile Inspections Collect data and photos directly from the field using your mobile device, even when you are working offline.
- Certification Tracking Manage complex certification cycles and automate renewal reminders so you never miss a critical deadline or expiration date.
- Corrective Actions Assign and track non-conformances and corrective actions to ensure your team resolves quality issues quickly and effectively.
- Configurable Checklists Build custom audit forms and checklists that match your specific industry standards and internal quality requirements.
- Automated Reporting Generate professional compliance reports instantly to share insights with your leadership team and demonstrate regulatory adherence.
Greenlight Guru Features
- Design Control Management. Build your Design History File and maintain a living traceability matrix that updates automatically as your project evolves.
- Risk Management Integration. Align your risk workflows with ISO 14971 standards to identify and mitigate hazards throughout the entire product lifecycle.
- Document & Change Control. Route documents for electronic signature and manage revisions with automated version control to ensure everyone uses the latest data.
- CAPA & Quality Events. Track corrective and preventive actions from start to finish with automated alerts that keep your team on schedule.
- Audit Management. Prepare for regulatory inspections with a centralized repository that allows you to pull required documentation in seconds.
- Training Management. Assign training tasks to your team and track completion status automatically to maintain a compliant, audit-ready workforce.
Pricing Comparison
Armature Pricing
Greenlight Guru Pricing
Pros & Cons
Armature
Pros
- Highly configurable interface adapts to unique organizational workflows
- Strong mobile capabilities for conducting audits in remote locations
- Centralizes all compliance documentation in one searchable location
- Automated notifications keep teams accountable for corrective actions
Cons
- Initial setup requires time to configure complex workflows
- Lack of public pricing makes budget planning difficult
- Interface may feel overwhelming for very small teams
Greenlight Guru
Pros
- Purpose-built specifically for medical device regulatory requirements
- Automated traceability matrix saves significant manual documentation time
- Excellent customer success team with deep industry expertise
- Intuitive interface compared to traditional enterprise QMS platforms
Cons
- Premium pricing may be high for early-stage startups
- Limited flexibility for workflows outside of medical devices
- Reporting tools can feel restrictive for complex data needs