Understanding eIFU for Medical Devices: A Comprehensive Guide Learn about the many options available for medical device labeling and how Weber Packaging Solutions can help you meet all
Scan for Safety The Future of Product Labels! #easymedicaldevice #medicaldevice What is an eIFU? and How do I create one?
In this episode, Monir El Azzouzi will summarize 2024 for Easy Medical Device and share projects for 2025. He will explain the Discover how Activem manages the complete lifecycle of your eIFU (electronic Instructions for Use). In this video, we walk through
An overview of US hernia and bariatric surgical products in the GORE GMP portfolio. Learn More Visit Highlights from La Rentrée du DM 2025 – Medical Device Made Easy Podcast
MedBoard EU - Joint clinical assessment procedure - EU 2025/2086 regulation for reimbursement in the EU: European Commission expands use of eIFUs | RAPS Want to access Sagemax Instructions for Use easily? No problem! Watch this video to discover two different routes to download
Are you trying to find a way to avoid printing your 362-page user manual for your medical device? The EU Medical Device Medical Device News March 2025 Regulatory Update
The European Commission has amended its implementing regulation to allow manufacturers to submit electronic medical device instructions for use (eIFU) to How Activem Digitizes, Stores & Hosts eIFU | Complete Digital IFU Management Solution
eIFU proposal until March 21st- eIFU for professional user Commission Implementing Regulation (EU) 2021/2226 Sagemax explains: Electronic Instructions for Use
What is an IFU and what is an eIFU (electronic instructions for use)? · What regulations and guidance apply to eIFU? · What are the benefits and Discover EasyIFU — the all-in-one platform for creating, managing, and distributing electronic Instructions for Use (eIFUs) and
e-IFU for medical devices - Consultation ongoing Medical Device News November 2025 Regulatory Update JavaScript is disabled. In order to continue, we need to verify that you're not a robot. This requires JavaScript. Enable JavaScript and then reload the page.
eIFU isn't just about storage — it's about traceability. Each version matters: v1, v2, v3… and regulators want to know why they Commission Implementing Regulation (EU) 2025/1234 of 25 June 2025 amending Implementing Regulation (EU) 2021/2226 as regards the medical devices. Health Data Legislation - Manufacturers should comply
Having regard to Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive The Update. Commission Implementing Regulation (EU) 2025/1234 (which amends eIFU Regulation) is available: HERE. Which devices are included Gore Medical Products Video
Medical Device Labeling 📢 New eIFU regulation alert! Electronic Instructions for Use: Capitalizing on the EU's eIFU Rollout | Michael Kania (Meddevo)
Regulatory Information Management Software Electronic Instructions for Use (eIFU) are no longer optional—they're the smart choice for medical device manufacturers in 2025.
Why Switch to eIFU?Top Regulatory & Operational Benefits Explained for Medical Device Manufacturers Commission Implementing Regulation (EU) 2021/2226 of 14 December 2021 laying down rules for the application of Regulation (EU) 2017/745.
Free eIFU Trial with EasyIFU Experience an easy, compliant way to manage electronic Instructions for Use (eIFU). ✓ Fully EasyIFU – The Smart Way to Manage eIFUs and Labels | Compliant with EU MDR Happy New Year 2022. All my best wishes for this year. For all the updates. check the links below.
This session presented by MedTech Leading Voice and AKRA TEAM, brings together top regulatory experts to unpack the EU's Untitled
Implementing regulation - 2021/2226 - EN - EUR-Lex Navigating the eIFU Regulation 2025/1234: Strategic Implementation Across Product Portfolios
UDI Beyond the Basics - A Masterclass on the Evolution of UDI Demand for regulatory information management software is growing due to increasing compliance requirements from health (eIFU) for medical devices used by Implementing Regulation 2021/2226 was intended to generally continue to advance Regulation
EU e-IFU for medical devices - Consultation ongoing: Regulatory bodies, device manufacturers, healthcare providers and numerous other stakeholders are gearing up for global
EU Opens Consultation on Draft Legislation for Electronic IFUs The September 12, 2025 Friday In-Focus replay from the MedTech Leading Voice Exchange (MLVx) features a focused
Thank You for Your Support! #easymedicaldevice #medicaldevice #regulatorycompliance Unlocking Flexibility with SmartEye! #easymedicaldevice #medicaldevice #regulatorycompliance New eIFU regulation alert! As of 2025, the EU is officially encouraging digital Instructions for Use (IFU) with the new regulation
Medical Device News JULY 2025 Regulatory Update Easy Medical Device Great Summary 2024 The current regulation (EU 2021/2226) specifies that not all medical devices can replace paper-based instructions with eIFUs. Only certain
eIFUs Now Allowed for All Professional Use Devices: EU Amending 💡 Free eIFU Trial with EasyIFU eIFU Requirements: Essential Guide for Medical Devices
Medical Device News - January 2022 Update 🔐 eIFU isn't just about storage — it's about traceability. In this special episode, we summarize the key takeaways from La Rentrée du DM 2025 — one of France's top MedTech regulatory
MedTech Europe response to electronic Instructions For Use (eIFU Implementing regulation - EU - 2025/1234 - EN - EUR-Lex
MedTech Europe warmly welcomes the European Commission's proposal for the update of the EU Regulation 2021/2226 laying down rules for the Regulatory Round-Up 2025 | MDR, IVDR, AI Act, UK PMS, FDA UDI & More! Welcome to your essential 2025 update on Sponsor • Medboard: Europe •Health Data Legislation - Manufacturers should comply: