We fast track your medical device compliance:
Complying with medical device regulations is costly and time-consuming, with companies spending up to €1.5M and 2 years on compliance before they can launch. Without alternative solutions, companies typically hire consultants and commit their teams to thousands of hours of manual work.
We make it simple:
Regulatory Requirements: vencot automatically scans and identifies specific regulatory requirements for each medical device, providing a clear list of tasks to ensure all standards are met.
Documentation: vencot automatically generates all necessary regulatory documents, eliminating manual errors and speeding up the preparation process.
AI- Copilot: Our AI copilot delivers tailored regulatory expertise for each product, offering precise and personalized on-demand guidance.
Real-Time Monitoring: Stay compliant with real-time regulatory monitoring and alerts, ensuring continuous adherence to evolving standards.