ON-DEMAND VIRTUAL CONFERENCE: The 12th annual UDI Conference was hosted virtually by USDM Life Sciences and moderated by Jay Crowley, the original developer and author of the FDA’s UDI requirements. Watch now.
ON-DEMAND WEBINAR: Currently, multiple regulators have or are launching national UDI Databases (US, EU, SFDA, NMPA, KFDA, HSA). Other regulators are following close behind. The new UDI challenge for device manufacturers is creating and submitting the required data to these national databases and maintaining this data – and regulatory compliance – over time.
Join USDM's Jay Crowley to discuss the growing UDI landscape, the similarities and differences of various UDI regulations, and their impact on MedTech organizations.
Learn how to comply with SFDA UDI requirements for medical devices in Saudi Arabia. Understand deadlines, database submissions, and labeling guidelines.
