marcus evans, the leader in Medical Device Quality Assurance Meetings, will host the 3rd Annual Medical Device Safety Monitoring & Reporting Conference, January 21-22, 2015 in Las Vegas, Nevada.
Via single track, case study presentations, panel & roundtable discussions, the meeting will identify relevant issues that medical device manufactures are facing in regards to safety and reporting protocols
Attendees will gain an understanding of the relevant issues that medical device manufactures are facing in regards to safety and reporting protocols. They will learn about emerging trends in global reporting, uncover repeatable models for efficient and timely reporting processes, implement strategies for safer device design, and emphasize the importance of a risk-based approach to post-market clinical trials for design safety.
On site, join Directors of Regulatory Affairs, Quality Assurance and Medical Device Reporting from the likes of GE Healthcare, Edwards Lifesciences Corporation, Fresenius USA Manufacturing, and many more!
Attending this conference will enable you to:
- Structure a Reporting Practice to Meet the Demands of the Increased Reporting Levels
- Assess the Impact of Increased Scrutiny on the Awarding of Substantial Equivalence in 510(k)
- Embed a Safety-First Design Process the Addresses Patient Safety while Advancing Organizational Goals
- & much more!
The 3rd Annual Medical Device Safety Monitoring & Reporting Conference was fashioned from direct feedback from past delegates who attended previous Medical Device Safety meetings, along with other events in the marcus evens Life Sciences series, including Medical Device Labeling.
For more information on this conference & to get a complete list of speakers or sessions, click on the conference brochure: http://www.marcusevans-conferences-northamerican.com/MDS_Oct30 or email Abby Wilson, Marketing & PR Coordinator at AbbyW@marcusevansch.com.