Sparta Systems to Offer Strategies for Electronic Regulatory Reporting at 2nd Annual Innovations in Medical Devices Conference

Holmdel, NJ Feb 25, 2011 – Sparta Systems, Inc., the maker of TrackWise® quality management software and the market leader in enterprise quality and compliance management solutions, today announced that it will present at the 2nd Annual Innovations in Medical Devices conference in a session titled “Regulatory Reporting for Medical Device Companies” on Friday, Feb. 25, 2011, from 11:15 a.m.-12:15 p.m. The event, taking place in Berlin, Germany, will present attendees with proven strategies for implementing an electronic reporting platform.
As global regulations for the reporting of adverse events and incidents in medical device manufacturing become increasingly stringent, more organizations have recognized the benefits of transitioning to electronic systems to track and manage the necessary data for reporting of these incidents. While transitioning to an electronic system for device reporting provides numerous benefits, such as increased efficiencies and improved accuracy of reports, the process can appear to be a daunting and complex challenge for companies seeking to make the switch. This panel discussion will offer attendees best practices for selecting and implementing an electronic medical device reporting solution. The panel, made up of esteemed industry experts, will share experiences and advice for deploying such a solution and gives attendees a roadmap for implementing their own electronic reporting system.
WHO: Moderator:
Joe Goodman, Manager, Solutions Consulting, Sparta Systems
Matthias Buerger, Vice President, Quality Assurance and Regulatory Affairs, EMEA, Zimmer
Ursula Morjaria, Director, Clinical Affairs, GE Healthcare
WHEN: Friday, Feb. 25, 2011, 11:15 a.m.-12:15 p.m.
“Regulatory Reporting for Medical Device Companies”
WHERE: Steigenberger Hotel Berlin
Los-Angeles-Platz 1
10789 Berlin, Germany