SESSION HIGHLIGHT:
European Medical Device Regulation Conference

July 13-14, 2017 | Arlington, VA

Hyatt Centric Arlington

Please Complete the Form to Download the Agenda

PRACTICAL CASE STUDIES: REGULATORY STRATEGY RESTRUCTURING IN LIGHT OF THE NEW RULES

• Evaluating the impact on all levels of the corporation
• Integration of flexibility in regulatory planning
• Timelines for compliance & impact on budget
• Deploying regulatory changes within corporate departments

JOHNSON & JOHNSON CASE STUDY: Glenda C. Marsh, Senior Director Global Policy Implementation

VARIAN MEDICAL SYSTEMS CASE STUDY: Peter J. Coronado, Director, Regulatory Affairs

Q1 has over a dozen years of experience in providing high level educational content for the European Medical Device Industry and is consistently ranked by participants as delivering quality program content, speaker selection, and facilitation.

Download the agenda to see all the presentation topics, speakers and formats.

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