ABOUT THE CONFERENCE

As medical device and diagnostic manufacturers continue to develop life enhancing products for patients around the world, product labels and instructions for use hold an increasingly important position in providing critical information to healthcare professionals and patients, focused on the safe handling and use of devices. Labeling executives strive to continuously optimize operations, ensuring a streamlined approach to label data collection, real estate formatting and regulatory reviews, and face numerous challenges in achieving each step in-line with regulatory requirements. Risk-based approaches to error minimization in label development and production is at the forefront of labeling team goals, which involves a cross-functional approach to ensure labels and instructions are compliant and intelligible, regardless of the intended user.

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 and instructions for use of medical products, meeting evolving regulatory guidance. With presenters bringing hundreds of years of combined experience to the educational platform, attendees with the following job functions will find this meeting of tremendous value:

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

ABOUT THE CONFERENCE

As medical device and diagnostic manufacturers continue to develop life enhancing products for patients around the world, product labels and instructions for use hold an increasingly important position in providing critical information to healthcare professionals and patients, focused on the safe handling and use of devices. Labeling executives strive to continuously optimize operations, ensuring a streamlined approach to label data collection, real estate formatting and regulatory reviews, and face numerous challenges in achieving each step in-line with regulatory requirements. Risk-based approaches to error minimization in label development and production is at the forefront of labeling team goals, which involves a cross-functional approach to ensure labels and instructions are compliant and intelligible, regardless of the intended user.