Medical Device Labeling Services, label changes, Management

Medical device manufacturers face an array of challenges in delivering their products to domestic and international markets. With potential risks to patient safety, Regulatory review, and ultimately brand equity, organizations must ensure that labeling documentation complies with the current product standards prevalent in each country distributing their devices. It is also necessary for these organizations to adopt practices that enable them to react quickly in order to process change requirements.

For medical device manufacturers, the definition of labeling includes any type of packaging or product identification, as well as anything that describes the product, its capabilities, and its intended use. This varied definition multiplies the challenges usually faced while attempting to meet international Regulatory compliance. While identification and other international safety standards assist in tracking products through the global supply chain, a variety of such standards in use today only complicate harmonization efforts further. For manufacturers, the supply chain can include contract manufacturers, private label and re-label partners, distribution points, and point- of- use healthcare providers. ​

Medical Device Labeling services

With a comprehensive knowledge of global medical devices market clubbed with proven expertise in Regulatory services, Freyr offers end-to-end labelling services that span across updating, reviewing, analysing, tracking and maintaining label changes.