Accelerating EU MDR Compliance: Regulatory Essentials for Medical Device Companies
Tips for Medical Device Compliance Success
Navigate the complexities of EU MDR compliance with our comprehensive industry brief. Discover key changes to the regulation, essential requirements, and strategic tips to ensure your medical devices meet EU regulatory standards. From premarket obligations to postmarket surveillance, learn how to streamline your compliance processes. Download the comprehensive industry brief now to accelerate your path to EU MDR compliance and maintain market access for your medical devices.
- What has changed in the EU MDR and how it will impact medical device companies.
- Essential steps for achieving and maintaining regulatory compliance in the EU.
- How digital solutions can simplify and optimise your EU MDR compliance efforts.
You'll learn:
Trusted By
Digital QMS: The Key to EU MDR Compliance
In the rapidly evolving medical device regulatory landscape, a robust digital quality management system (QMS) is crucial for EU MDR compliance. As the updated requirements demand more stringent documentation, risk management, and postmarket surveillance, traditional paper-based systems fall short. A proven digital QMS like MasterControl Quality Excellence streamlines compliance processes, ensuring real-time data access, efficient document control, and seamless integration of quality and regulatory activities. By adopting EU MDR software tailored for medical device regulatory compliance, companies can navigate complex requirements with greater ease and confidence.
See what our users are saying
EU MDR Compliance FAQs
What are the key changes in the updated EU MDR guidelines?
The main changes to the regulation include more premarket and postmarket obligations, stricter risk management requirements, new device identification and traceability rules, expanded device classifications, and new QMS compliance requirements.
How does EU MDR affect medical device classification?
EU MDR updates have introduced new device classifications, including a new Class I category (Class Ir) for reusable devices. Some devices may be moved to higher risk classes, and the definition of medical devices has been expanded to include certain non-medical and cosmetic devices.
What is EUDAMED and how does it impact manufacturers?
The European Database on Medical Devices (EUDAMED) is a central repository for information on medical device life cycles. Medical device companies will need to enter reports of incidents, injuries, and deaths involving their devices into this database.
How can digital solutions help with EU MDR compliance?
Purpose-built digital QMS solutions, such as MasterControl Quality Excellence, optimise compliance processes by providing real-time data access, more efficient document control, and seamless integration of quality and regulatory activities. These modern systems make it easier to meet the EU MDR’s stringent documentation and risk management requirements.
Get EU MDR Ready Now
Simplify your medical device regulatory compliance journey with our expert guide.
Download the EU MDR Industry BriefMasterControl: Your Partner in EU MDR Compliance
MasterControl's fully connected QMS platform empowers medical device companies to streamline processes, ensure data accuracy, and maintain compliance with the EU MDR.
-
Streamlined Processes:
MasterControl's intuitive interface and automation capabilities help you optimise processes, reducing manual tasks and errors while accelerating time-to-market.
-
Data Accuracy:
Ensure data integrity and traceability throughout your product life cycle with MasterControl's robust data management features.
-
Regulatory Compliance:
The MasterControl platform is designed to help companies meet the stringent requirements of regulations like EU MDR, including functionality built for risk management, clinical data management, and postmarket surveillance.
-
Enhanced Visibility:
Gain real-time insights into your operations with MasterControl's advanced analytics and reporting tools that enable you to identify potential risks and take more proactive measures.
Learn More About Regulatory Compliance
Talk to a Compliance Specialist
Contact one of our experts today to see how advanced digital solutions can ease your compliance burdens.
