Med Device Link - May 2023
LexisNexis Reed Tech
Regulatory compliance and product data management solutions for medical device manufacturers and pharmaceutical labelers
Hello! We are looking forward to a summer of informative webinars, in-person conferences and UDI regulatory updates. We continue to monitor global health authorities and will keep you in the know as new information becomes available.
Next month, we will?give an update on our latest alliance with RegDesk?, a top-rated AI-powered RIMS platform with all the tools you need to maintain global regulatory compliance.
?As always, we are here to help you monitor developments with UDI requirements. Don't hesitate to reach out to us via email at: [email protected] if you have product data management questions.?
Ask the Experts: What should I know about the EU Legacy Medical Device Amendment?
In recent news, the European Commission enacted an extension to the transition deadline for Legacy Medical Devices to be placed on the EU market. In this webinar, UDI experts Gary Saner and Ronald Boumans answer questions about this decision and how it affects medical device manufacturers.
In Person Conferences and More!
The Reed Tech Life Sciences team is looking forward to a full calendar of upcoming Med Tech events. Visit our website to see where you can find us this summer and beyond.
EU Amendment to Extend Legacy Medical Device Transition
The European Commission proposed an extension to the transition deadline for Legacy Medical Devices to be placed on the EU market. Here is a quick summary of recently posted information, and a short video with Gary Saner talking through the updates.?
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Introducing the 'Understanding UDI Series'
Access the 'Understanding UDI Series' for short tutorials and quick reference slides. Learn more about regulations, requirements and timelines for Global Health Authorities. See how you score on the quiz!?
Takeaways from RAPS Euro Convergence
Greetings from Amsterdam!
Sales Development Representative, Miriam Kniering attended the RAPS Euro Convergence conference in Amsterdam. We asked her a few questions about her experience and key sessions she attended.?
Risk Solutions for Med Tech
Our partners at Greenlight Guru just announced a new product offering: Risk Solutions for MedTech. Improve the risk management process with a first-of-its-kind, complete risk management software. Leverage AI-generated insights with intuitive workflows, aligned with ISO 14971:2019, for streamlined compliance and reduced risk throughout the entire device lifecycle.
Questions? Ask the Experts
If your team has questions about health authority requirements, device classes, Unique Device Identification (UDI) data attributes, or related topics, get in touch! We'd be happy to help.