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Enabling Product Data Availability for GS1 Compliance

Enabling Product Data Availability for GS1 Compliance

Medical device manufacturers know the compliance side of UDI data well. But what happens after you meet the regulatory deadline? The answer lies in a concept many teams are only beginning to plan for: product data syndication — the process of sharing accurate, consistent device data with every downstream stakeholder who needs it. From hospital systems and group purchasing organizations (GPOs) to patient electronic...

Henry Schein: UDI Data Submission Case Study

Henry Schein: UDI Data Submission Case Study

Jeff Peacock, VP of Global Quality Assurance and Regulatory Affairs at Henry Schein, gives industry members an overview of how his organization approached the challenge of UDI data submission to FDA. Download the guide to learn about: The challenges presented by the UDI data submission mandate How Henry Schein approached the problem of data collection and standardization Why Henry Schein chose the...

How Cadwell Implemented a UDI Strategy Customized for a Diagnostic Technology Manufacturer

How Cadwell Implemented a UDI Strategy Customized for a Diagnostic Technology Manufacturer

How a neurotechnology manufacturer leverages LexisNexis Life Sciences Solutions SingleSource ™ for Medical Devices Cadwell is a global medical device company founded after their creation of the world’s first microprocessor EMG. In 2019, they celebrated 40 years of delivering innovative neurodiagnostic, neuromonitoring, and sleep diagnostic solutions to the world. Cadwell sought an experienced vendor...

LexisNexis Life Sciences SingleSource for Drug Products and Schlafender Hase TVT, the Text Verification Tool

LexisNexis Life Sciences SingleSource for Drug Products and Schlafender Hase TVT, the Text Verification Tool

LexisNexis Life Sciences Solutions and Schlafender Hase ® are leaders in the life sciences industry, working together to help ensure that pharmaceutical companies and their products are compliant with global regulatory standards. Both companies understand and solve industry challenges with responsive solutions. Industry Challenges Pharmaceutical companies operate in a highly regulated industry with countless...

How Kenmark Eyewear Created a UDI Strategy for Current and Future Challenges

How Kenmark Eyewear Created a UDI Strategy for Current and Future Challenges

How a global provider of world-class eyewear brands leverages LexisNexis Life Sciences Solutions SingleSource ™ for Medical Devices Kenmark Eyewear is an employee-owned company headquartered in Louisville, Kentucky with many eyewear consultants across the U.S. and abroad. Their company is passionate about quality products, original designs, high ethical standards, sustainable practices, innovative marketing and...

How to Gain Regulatory UDI Submission Efficiencies with LexisNexis SingleSource for Medical Devices

How to Gain Regulatory UDI Submission Efficiencies with LexisNexis SingleSource for Medical Devices

How a global respiratory device manufacturer built regulatory UDI expertise with LexisNexis Our customer is a global respiratory solutions provider, dedicated to supporting and improving the lives of patients. With several acquisitions over the past decade, they have grown to approach the size of a billion-dollar company with tens of thousands of SKUs sold in more than 100 countries. They are focused on innovation to...