[akehrer]

First of all, thank you Shift Labs for putting up their information and helping make confusing regulatory processes clearer.

Secondly, I want to let people know my company[1] works with many start-ups in the medical device space that are developing regulated products, both 510(k) and CE mark. We are engineers that understand the regulatory process not just regulatory consultants.

If anyone is interested feel free to contact me [e-mail].

[1] http://www.in2being.com/