Med Device Link Newsletter-February
LexisNexis Reed Tech
Regulatory compliance and product data management solutions for medical device manufacturers and pharmaceutical labelers
Hello!
We have hosted a couple of informative presentations this month with updates on UDI and global health authorities. Check out the materials below. We are closely monitoring the recent proposal for EU legacy devices and timeline extensions plus the progress with Australia TGA.??
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.
Check out some interesting statistics about UDI submitted to GUDID by class of device. Did you know? Reed Tech annually submits about 1 in 4 electronic records to GUDID.
RECENT WEBINARS
China's Expanding UDI Requirements for Medical Devices
UDI data requirement expert Gary Saner of Reed Tech and China regulatory consultants Hamish King and Victoria Caldy of Cisema discuss best practices for manufacturers to comply with current and emerging UDI and medical device registration mandates in China.
Global UDI Update with Dental Industry Specifics
Reed Tech hosted an informative webinar discussing UDI for US and global health authorities, with specifics on the impacts to the dental industry.
领英推荐
Medical Device News
EU Proposal 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 about the reasoning behind this decision and how it affects manufacturers.
2023 MedTech Industry Benchmark Report
Greenlight Guru just published the?4th Annual Medical Device Benchmark Report, with data gathered from 600+ medical device professionals to better understand the state of the industry in 2023. Discover the latest insights on the challenges, strategies, and best practices that shape the medical device industry.
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.