Spend your time on Innovation, don’t spend it worrying about compliance
Ryden’s AI platform helps you become and maintain compliance quicker across all your regulatory requirements across all your facilities to spend more time on what really matters.
Revolutionize Your Quality Management and Regulatory Compliance
Use Cases
Supplement or even replace your internal audits and supplier audits. No more pulling employees off their roles to be an auditor for a week!
Regulatory monitoring and new requirement gap analyses
Prepare for premarket submissions and globalization
Process improvement recommendations
How we build AI to service you
• Our expertise is the difference. We do not have the AI do a key word search! Our team trains the AI on our collective experiences being on the front line in inspections, customers, auditors, etc.
• Our approach yields extremely accurate outputs. 96%+ accuracy on AI- observed gaps across 1,000+ assessment questions.
• Our system runs in the background informing you specifically where you are noncompliant before you even know to ask!
• Our system combs through new and updated requirements across all major jurisdictions (USA, Canada, EU, Australia, etc.) and tailors notifications to what could be impacting you.
• We promote an enterprise holistic view showing opportunities found across regulations, across departments or across facilities at a corporate level. This aids in resource planning and mentorship opportunities.
Value for MedTech companies of all sizes
Startups
If your company is new to the MedTech space or just getting ready to take a product to market; don’t waste money applying for approval till you have used our solution to validate your product compliance.
Mid-size
With built-in project management tools, you will be able to streamline compliance across projects and regulatory requirements. Forecast compliance dates, burndown charts, and assign corrective actions to specific people.
Enterprise
Dashboards give insights to all your facilities world-wide. Ensure corporate policies are being implemented properly. Consolidate supplier qualifications and ongoing audits which is especially useful for suppliers shared across facilities.
Be Proactive, not reactive
Don’t wait till the FDA is at your doorstep to do an audit. Let us schedule a demo of our solution and show you how we will change the way you handle compliance.