European Medical Device Regulation Conference
July 13-14, 2017 | Arlington, VA
Hyatt Centric Arlington
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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.
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