The global healthcare industry is transforming—quickly transitioning from proprietary solutions to a foundation of open, global GS1 standards.
Since 2015, medical device manufacturers have been scrambling to ensure they are successfully complying with various governments’ rules, regulations and timelines for Unique Device Identification (UDI). Moreover, they often use multiple systems to do so, and as a result, duplicate efforts instead of boosting efficiencies!
Different rules in different countries pose unique challenges to medical device companies. Meanwhile, more and more agencies will be implementing new rules over the next 5 years—and manufacturers often find themselves feeling in the dark with what these requirements are and how regulators want to receive them.
While the industry has achieved many milestones, there are a lot of unanswered questions in the healthcare realm. Join us for a compelling webinar where you will learn the answers to:
- How are companies successfully creating, updating and sharing UDI data?
- What systems, processes and tools are helping manufacturers satisfy individual data needs of both regulators and customers?
- Where can people go to get educated, find best practices and drive efficiencies?
Speakers: Jason Gunn and Mike Crabb
When: Thursday, March 25 at 11 am CET
Did you ever want to learn how GS1 Member Organisations provide healthcare data connectors to Healthcare regulatory and commercial authorities? How global healthcare purchasing organizations, hospitals use data models to receive data from datapools? This is your chance! This is the time to learn to show your members direct value.
In this short but intense session, you will discover...
- Latest developments in healthcare,
- Important aspects to consider about data models in healthcare,
- How to connect easily to UDI regulatory databases (e.g. GUDID, EUDAMED, etc.)
- How to use GDSN and healthcare connectors.
We open the floor for you to ask our experts all your burning questions!
When: February 24th at 12:00 pm (UTC-5 time)
You want to attend but have calendar conflicts? Register anyway, and we will send you the webinar recording after the meeting.
The deadline for implementation of traceability solutions for Medical Devices and In-vitro Devices is just around the corner. However, the MDR and IVDR regulations raise certain questions and challenges for manufacturers, importers, and authorized representatives.
SoftGroup and GS1 Bulgaria have teamed up to provide a compact and understandable overview of the most important regulatory updates as well as the specific UDI requirements.
When: 26th November 2020, at 10 a.m. EEST
Governments, regulators, hospitals and retail pharmacies in more than 70 countries are driving implementation of GS1 standards in healthcare and many of the implementations require solution providers to support GS1 standards in their systems and processes to provide appropriate solutions to their customers.
GS1 Healthcare will soon give the access on its Solution Partners webpage to an interactive map which will display all our Solution Partners per country.