With over 20 years in regulated medical device development and manufacture, my experience spans every facet of a product's lifecycle. From development and mechanical testing, to clinical testing and the FDA and EU approval processes, to scaled manufacturing, labeling, and distribution, to post-market surveillance, I've planned it, written it, executed it, gained approval of it, and managed it. I've built the infrastructure to support it, and saved the companies for which I worked cash at every point along the way.
My abilities took me from being a temporary employee all the way to Executive Vice President of two Fortune 500 companies. I do in minutes what others take hours to do, and I do it right.
If your opportunity has the right energy and purpose, I'll give you everything you'll need to be successful, sooner than anyone else, and at the lowest aggregate cost.