Second Annual Medical Device Summit - Jack McLane to present Risk Assessment workshop : March 7-8, 2011

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: