marcus evans, the world's largest event management group, will host the 4th Annual Medical Device Safety Monitoring & Reporting Conference in Las Vegas, NV on January 27-28, 2016. This 4th event will focus on key updates and advancements in medical device safety, medical device reporting, eMDR, post market-surveillance, complaint handling, audit handling and national & international standards.
Previous attendees include:
Omnyx, LLC, Stryker Medical, St. Jude Medical, Fresenius Medical Care North America-Global Manufacturing Operations, Covidien Surgical Solutions, Cardinal Health, Allergan, Abbott Medical Optics, Inc., Boston Scientific CRM, Nihon Kohden, Novocure, Terumo BCT, and many others.
This 4th Annual Conference will enable you to:
- Develop a cohesive medical device reporting (MDR) model that will comply with FDA standards
- Implement a robust electronic medical device reporting (eMDR) program to achieve FDA MDR compliance
- Remain vigilant with post market surveillance data accumulated to ensure all generated information is documented
- Manage complaint handling effectively to ensure accurate data accumulation
- Establish a robust audit preparation plan in anticipation of future audits
Featuring Case Studies from Leading Professionals, including:
Bill Maloney, Physicist, MDR Policy Branch - Office of Science & Biometrics Center for Devices & Radiological Health, Food and Drug Administration
Darin S. Oppenheimer, RAC, Director, Global Regulatory Affairs, Baxter Healthcare Corporation Karen Smith, Director of Regulatory Compliance, BD MPS
Sharon Perez, Ph.D., Director, Global Medical Device Safety, Novocure Marcelo Trevino, Senior Director, Quality & Regulatory Affairs, Nihon Kohden
For more information on this conference or to get a complete list of speakers, sessions or past attendees, visit the conference website, or email Nicolette Fiordirosa, Marketing & PR Coordinator at nicolettef@marcusevansch.com