Innovatum Sponsors UDI Beyond the Basics Masterclass
Innovatum invites you to take advantage of this free 2-hour UDI Masterclass we sponsored that was conducted by FDA and noted industry experts including Jay Crowley…
Topic
Unique Device Identification (UDI).
UDI requirements across FDA GUDID, EU EUDAMED, Brazil ANVISA and China NMPA, and how one product record can satisfy all four.
26 articles on UDI.
Unique Device Identification Webinar May 13, 2021
Join us May 13, 2021 for A Discussion of the Requirements, Challenges, & Opportunities of Unique Device Identification (UDI).
Innovatum CEO Ardi Batmanghelidj to Speak at Packaging & Labeling Regulations Webinar
Innovatum President and CEO, Ardi Batmanghelidj, will be discussing UDI-MDR requirements as part of the upcoming Orange County Regulatory Affairs (OCRA) webinar…
9th Annual Q1 Device and Diagnostic Labeling Conference
Innovatum, a proud sponsor of the **9th Annual, Q1 Medical Device and Diagnostic Labeling Conference in Chicago, May 14-15**, invites you to join this conference at a…
5 Unique Device Identification Challenges
Many of FDA's UDI requirements have already phased in, so Packaging Digest lists the top 5 unique device identification challenges.
Innovatum Announces ISO 9001:2015 Certification and EU MDR/IVDR Solutions at the 2018 UDI Conference
At the 2018 UDI Conference, Innovatum, Inc. is pleased to announce ISO 9001:2015 Certification by an ANAB accredited body for its quality management system for…
Innovatum Makes Cover Story of Major Life Sciences Industry Publication
Innovatum further demonstrates its leadership role in the Life Sciences labeling niche by contributing the cover feature article in Medical Design Briefs.
What I Learned While Presenting in Front of the FDA About UDI Management
I was invited to speak at a UDI-centric conference on behalf of AIM North America Healthcare Committee about UDI management software & other technologies.
Taiwan’s Version of Unique Device Identification
Taiwan is progressing in the area of Unique Device Identification, having produced a guidance document late last year. The document references US FDA rules
Innovatum, Silver Sponsor and Speaker at 3rd Semi-Annual Medical Device & Diagnostic Labeling Conference
Innovatum is a Silver sponsor at the 3rd Semi-Annual Medical Device & Diagnostic Labeling Conference taking place Sept. 24-25, 2015.
Real Benefits of UDI in the Operating Room and Beyond
One of the benefits of UDI is combatting counterfeit products. Counterfeit medical devices create many problems for patients, caregivers and providers.
UDI Implementations In Full Swing With Innovatum
Innovatum if off to a great start this summer by managing seven global labeling UDI implementation projects and customers are taking advantage of their intensive…
2015 UDI Conference Highlights
The 2015 UDI Conference had record participation, but many Medical Device Manufacturers were not able to attend. Here are the UDI Conference highlights.
Medical Device Labeling Guidelines
Our expert team at Innovatum are dedicated to meeting the compliance challenges of highly regulated industries such as pharmaceuticals and medical devices.
Understanding Unique Device Identification
Our experts at Innovatum can help you with all you need to know about unique device identification (UDI) so you are complying with the FDA regulations.
Understanding the Difference between Class I, Class II and Class III Medical Devices
There are three FDA device classifications Class I, Class II, and Class III based on the risks of each device. For more information, visit our website.
Understanding the FDA UDI Final Rule
The Unique Device Identification system and Global Unique Device Identification Database increase safety in healthcare. Visit us to learn more about them.
What is Unique Device Identification?
Unique Device Identification is intended to enhance the safety of healthcare workers, patients and caregiver. Visit us to learn more.
The FDA’s UDI System is a Historic Point in Medical Safety
The first phase of the FDA’s unique identification (UDI) system marks an historic point in medical safety. Visit us today to learn more.
What Are My Options for Medical Device Labeling
The Food and Drug Administration (FDA) has set specific standards for the labeling of medical devices. It is vital that medical devices are labeled clearly and…
Is it a Requirement to Label Class III Medical Devices?
Class III medical devices require the most rigorous monitoring because they present a “high risk” when it comes to patient safety. Learn more here.
Innovatum President To Present At 2014 FDA UDI Conference
Innovatum’s President and CEO Ardi Batmanghelidj has been asked to speak on the topic of UDI at the October 28 – 29, 2014 FDA UDI Conference in Baltimore, Maryland.…
Innovatum President Serving as 2014 Chair of AIM’s North American Healthcare Committee
AIM, the worldwide association for Automatic Identification and Mobility announced today that Innovatum’s President, Ardi Batmanghelidj, is serving as Chair for the…
QuickLabel Systems And Innovatum Present Jointly
Ardi Batmanghelidj, President of Innovatum and Eric Pizzuti, Vice President and General Manager of QuickLabel Systems recently conducted a presentation called,…
Astro-Med’s QuickLabel Systems Forges New Partnership With Innovatum
Astro-Med QuickLabel Kiaro Printer works with Innovatum's ROBAR
Innovatum Corporation Joins AIM – Signals Commitment to Automatic Identification and Mobile Solutions
Innovatum announced today that it has joined AIM, the worldwide association for Automatic Identification and Mobility. AIM works to increase the understanding and…
Other topics
- Enterprise labeling
- Compliance
- Regulatory submissions
- Labeling quality
- Pharmaceutical labeling
- Standards
- Supply chain
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