Medical Device Registration Tracking and Reporting

Streamlined Tracking and Reporting for Your Medical Device Registrations and Renewals

Replace spreadsheets and out-dated systems with powerful software that streamlines medical device registration tracking and reporting on a global scale

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Centralized Tracking and Global Reporting

Say goodbye to scattered data in spreadsheets and missed deadlines. Our platform centralizes your medical device registration information, giving you real-time visibility into global approvals and renewals while enhancing cross-functional team alignment. With automated notifications, you’ll stay ahead of renewal deadlines, reduce penalties, and streamline your entire registration process. Boost efficiency and manage global submissions seamlessly.

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Always-On Compliance Management

Take charge of compliance with proactive management. Automatically track product timelines and receive reminders for upcoming renewals and health authority responses. With real-time updates, medical device manufacturers can effortlessly stay compliant across global markets while ensuring uninterrupted patient access to your company’s innovative product.

Smarter Decisions with Real-Time Analytics

RegDesk’s reporting and analytics tools offer customizable reports and real-time insights into key metrics like submission times, costs, and statuses. With automated renewal notifications and performance tracking, teams can track KPI’s, optimize workflows, and stay ahead of deadlines to ensure compliance. These powerful tools help manufacturers make data-driven decisions, streamline operations, and minimize penalties.

Seamless Regulatory Management

RegDesk offers an intuitive interface with centralized registration management, easy data access, and customizable reporting. Ensure compliance and optimize workflows with real-time insights, automated renewal notifications, and KPI tracking. With advanced user management and robust analytics, RegDesk streamlines regulatory workflows, improving efficiency and reducing the risk of non compliance.

“RegDesk’s built-in reporting and statistics in their Tracking module allows our regulatory leader to easily present the KPIs to the organization. We are also able to keep track of the incoming international requests which allowed for our company to enhance its approach on global expansion.”

Olivia P., Senior Director, Regulatory Affairs

Large Medical Device Company

Put an end to costly delays!

Get Started with RegDesk and experience enhanced visibility, proactive compliance,
streamlined workflows, and powerful analytics for your team.

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More About Medical Device
Registration Tracking and Reporting

Navigating the FDA Medical Device Approval Process: A Step-by-Step Guide for Manufacturers

Navigating the FDA Medical Device Approval Process: A Step-by-Step Guide for Manufacturers

April 30, 2025

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TGA Guidance on UDI Timeframes

TGA Guidance on UDI Timeframes

April 22, 2025

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Impact of FDA Staff Cuts on Patient Access to Medical Devices

Impact of FDA Staff Cuts on Patient Access to Medical Devices

April 17, 2025

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