Medical Device and Diagnostic Labeling Workshop Intensive Agenda

Building on over a decade of educational platform development and delivery through the Annual Q1 Medical Device and Diagnostic Labeling Conference, this upcoming course will provide participants with concentrated educational deliverables focused on ensuring a seamless approach to label development, delivery and management. Given the many challenges faced by the industry; from bridging the gap between the manufacturer and the HCP or patient end-user, by conveying critical information focused on the safe handling and use of the product, to the formulation of information pertaining to the safe distribution, storage and use of the product, device and diagnostic labeling executives will gain tremendous value from interacting with like-minded executives. Gaining insight into how other organizations have implemented new EU MDR labeling provisions will provide attendees with an unrivaled educational opportunity. Hosted in San Diego this September, this one-time course will be of great interest to not only those local to the West Coast market, but also participants that were unable to join Q1 at the Chicago meeting hosted in May 2018.

Core Educational Objectives Include:

• Understanding the new EU MDR’s impact on labeling processes and practices
• Enhancing label compliance through international standards and requirements
• Label requirements in ISOs and applicability to operations and translation management
• Detailed analysis of regulatory intelligence collection and new requirement integration
• Best practices for US and OUS advertising/promotional labeling content compliance
• Practical industry insight into ELS (enterprise labeling system) implementation
• Rationale development for corporate buy-in of label management software
• UDI program developments, flexibility, and adaption to evolving global requirements
• Benchmarking opportunities with labeling professionals in a small, dynamic setting

WHO SHOULD ATTEND

Participants in the Medical Device & Diagnostic Labeling Conference will represent leading Medical Device Corporations concerned with the appropriate development, design and delivery of labels for medical products that meet expanding regulatory requirements. With presenters bringing dozens of years of combined labeling experience to the speaker platform, attendees with the following job functions will find this program of great interest:

• Labeling
• Document Control
• Regulatory Affairs
• Quality Assurance
• Packaging

Building on over a decade of educational platform development and delivery through the Annual Q1 Medical Device and Diagnostic Labeling Conference, this upcoming course will provide participants with concentrated educational deliverables focused on ensuring a seamless approach to label development, delivery and management. Given the many challenges faced by the industry; from bridging the gap between the manufacturer and the HCP or patient end-user, by conveying critical information focused on the safe handling and use of the product, to the formulation of information pertaining to the safe distribution, storage and use of the product, device and diagnostic labeling executives will gain tremendous value from interacting with like-minded executives. Gaining insight into how other organizations have implemented new EU MDR labeling provisions will provide attendees with an unrivaled educational opportunity. Hosted in San Diego this September, this one-time course will be of great interest to not only those local to the West Coast market, but also participants that were unable to join Q1 at the Chicago meeting hosted in May 2018.