Accreditations, Approval and Notification
In addition, LNE is recognized by internationally as a top notified body for certification of quality systems and manufacturing processes. Our technical expertise and accreditations allow for one-stop regulatory certification in North America, Europe, Asia and other major world markets across a variety of industries. LNE/G-MED America is your local connection to LNE. Contact us for all of your testing certification and training needs. AccreditationsFor details on the below accreditations, see LNE: Accreditations, Approval and Notification.
For details on the below approvals and notifications, see LNE: Accreditations, Approvals and Notifications.
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- Progress Report - News
- MD Revisions Draft Amendments
- MD Classifications
- ISO 14971:2012
- MDD Revision: Actors, Roles and Responsabilities
- WEEE2 Directive
- Maintaining Compliance
- Revisions to the MDD
- ISO 13485 and FDA
- Controlling Outsourced Processes
- The Notified Body’s Role in Medical Device Certification
- EC Publishes E-Labeling Regulation
- IVD Updates
- Post-Market Phase
- IEC 60601 3rd Edition
- Tech File Evaluation
- Clinical Evaluation
- Recast of IVD Directive
- Own Brand Label Devices
- Software Engineering
- Med. Device Packaging
- Single Use Devices
- Usability Engineering
- FDA Use of ISO 13485
- Risk Management
- IVD Directive
- Switching Notified Body
- 60601 3rd Edition Status
- Regulatory News
- Ask Our Experts
- Free Guide: CE Marking
- Free Guide: IEC 60601 3rd Edition
- Free Guide: EMC Testing
- Free Guide: Brazil MD Approval
- Free Guide: Japan MD Approval
- Free Guide: IVD
- Technical FAQs
- Progress Report - News



LNE is a recognized notified body with more than 100 years of technical expertise. Through our nearly 150,000 square foot testing facility, manufacturers can obtain state-of the art evaluation and confirmation of their designs.


