IQPC announces the 13th Annual Software Design for Medical Devices conference taking place May 24th-26th at the The Westgate Hotel, San Diego, California.
This premier conference will gather industry leaders presenting on managing regulatory requirements and building quality into design.
The 13th Annual Software Design for Medical Device will feature an exceptional speaker line up, including Richard C. Chapman, BA, MS, General Engineer, of the U.S. Food and Drug Administration (FDA).
Mr. Chapman's presentation is just one of many informative and educational sessions at next month's conference in San Diego. Some of the other confirmed speakers include:
- Deborah Madsen, Senior Staff Engineer, Lead Auditor, Underwriters Laboratories
- Alex Grob, Director, Regulatory Affairs, GE Healthcare
- Paul Fernandes, Director, Software Development, U.S. Genomics
- Edmond W Israelski, PhD Human Factors Program Manager, Abbott
- Murali Janakiraman, Principal Engineer, Medtronic
- And Many More!
As they lead discussions on:
- Auditing Medical Devices Using Global Standards: A Notified Body / CE Perspective
- Adapting to Changes in the Medical Device Directive: A Case Study
- Achieving Shorter Development Cycles Without Sacrificing Compliance And Quality
- Human Factors Engineering in Designing Software
- Medical Device Interoperability - Integrating the Health Enterprise
Pharma IQ to organize 4th Improving Solubility conference at The Park Hyatt in Philadelphia