10th Annual Medical Device and Diagnostic Labeling Conference

May 6-7, 2020 | Chicago, IL

10th Annual Medical Device and Diagnostic Labeling Conference
May 6-7, 2020 | Chicago, IL

Access Agenda

WE GUARANTEE 100% PRIVACY, YOUR INFORMATION WILL NOT BE SHARED

“There are some viable solutions out there and it’s great to know how to tap into them and how others have done so. I gained much insight and useful information from others who attended and participated. It was a very nice event. Q1 did a great job coordinating it.”

Manager, Labeling & Packaging
Animas

“I took a lot of good and practical information out of the discussions, very useful.”

Manager, Technical Communications
Medtronic

“It was a fun to be part of a well-organized event and in the company of knowledgeable industry professionals, thanks again!”

International QA Compliance Manager
Instrumentation Laboratory

“The peer to peer conversations were great! I liked hearing the different feedback.”

Global Labeling Manager
Intuitive Surgical

“Great insight to other company experiences.”

Labeling Specialist
Edwards Lifesciences

About the Conference:

With the goal of ensuring safe use of medical technology, regulatory authorities on an international level continuously release new provisions impacting label content, prompting teams to develop increasingly flexible strategies in order to reach compliance in a timely manner. Labeling teams currently strive for a solidified approach to regulatory management, also encompassing localization and translation requirements as well as rapidly expanding market-specific UDI rules, to ensure a streamlined approach to the creation and delivery of comprehensive labels across the globe. To achieve success, use of state of the art technology has proven of great interest to the industry in the process of shifting towards ELS, CMS, or MDM solutions.

Core Topics to be Addressed:

EU MDR & IVDR impact on labels through Notified Body perspectives
Solidifying IFU content with enhanced human factors & technical writing
Optimizing labeling management for evolving industry regulations
Quality & compliance benchmarks for translation providers partnerships
Assessment of international UDI rules and preparing for implementation

Program Highlights:

Diverse industry and regulatory perspectives
Interactive discussions to foster collaborative exchange
Blend of large & small manufacturer perspectives
Technology exchange groups on labeling optimization

Core Topics to be Addressed:

EU MDR & IVDR impact on labels through Notified Body perspectives
Solidifying IFU content with enhanced human factors & technical writing
Optimizing labeling management for evolving industry regulations
Quality & compliance benchmarks for translation providers partnerships
Assessment of international UDI rules and preparing for implementation

Access Overview

WE GUARANTEE 100% PRIVACY, YOUR INFORMATION WILL NOT BE SHARED

Audience

75 Attendees

All attendees come directly from medical device companies

Distinguished Presenters

Speaker recruitment in process

Networking

Networking time is built into the agenda to allow industry peers to connect and exchange ideas

Open Dialogue and Group Share

Each presentation is followed by 10-15 minutes of open dialogue for questions and exchange of best practices

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