March 7-8, 2011
Omni Parker House
Boston, MA
Clinquest COO & Vice President of Regulatory Affairs John McLane will be presenting "Risk Management in Clinical Studies" at the Second Annual Medical Devices Summit.
- Use this intimate setting to ask questions about making your process 510(k) compliant
- Ask questions about preparing and conducting clinical trials for 510k and IDE devices and some of thepitfalls in assessing risks
- Use the rountable format to discuss more closely the ins and outs of risk management in the clinical setting
- Speakers: Dr. John McLane, VP of Clinical and Regulatory Affairs, Clinquest and Lisa Ferrara, CEO, OrthoKinetic Technologies
To register or for more details: http://www.opalevents.org/conferencehtml/past/medical_devices_summit/medical_devices_summit.php