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June 3, 2010
4:00pm-5:30pm
light reception will follow
Location:
BioHouston Office
2555 Holly Hall Street, Suite 100, Houston, TX 77054
Cost:
BioHouston Member- Free
Non-Members: $10
Questions?
Contact: Keisha Curtis Keisha.curtis@biohouston.org 713-979-9212
Presented by:
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Many US companies have found that marketing their medical device through European regulatory approval is a faster path to revenues.
Join us for an informative seminar that will provide advice and a roadmap from a European device regulatory expert, an Authorized Representative and a US company that has successfully received their CE Mark, and completed an audit.
If your company is looking to market your product in Europe, or learn about the March 2010 changes to the regulations, you will not want to miss this seminar.
Speakers:
Carla Kikken-Jussen, President & CEO, Meditech Strategic Consultants
Dr. John O Dwyer, European Manager & Medical Director, National Standards Authority (NSAI)
Mike Lowe,CEO, OrthoAccel Technologies
Sponsored by:
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