Sectors:
Locations:
Min Investment:
Max Investment:
Target Investment:
Master of Business Administration (M.B.A.)
2017
MedTech Impact Partners is a medical device regulatory strategy consulting firm that partners with some of the most innovative medtech companies and investors to navigate the FDA.
2018
Wavemaker Three-Sixty Health is the leading U.S. seed stage venture capital fund focused 100% on healthcare. The fund is backed almost exclusively by healthcare LPs - both leading organizations and prominent individual executives - across payers, providers (across the continuum of care), and pharma. This gives the fund a unique advantage with respect to identifying, evaluating, and, most importantly, supporting early-stage healthcare technology companies.
2021
2023
2023
2022
2022
2015 - 2017
2015 - 2017
Our Department was engaged. We experienced an annual increase in department engagement, culminating in best-in-class scores. Product Launch - I led a cross-functional team as senior champion for product launch in China. We developed an integrated plan including Go-To-Market, Manufacturing, and Regulatory approvals. Change Management - I was the senior leader responsible for a team of 30 permanent and temporary associates in an accelerated 4-month compliance resolution project. I led an evaluation of over 10,000 records ahead of schedule mitigating significant business risk. Budget Development / Management - I instituted a regular budget development and review process in concert with finance partners. We realized on-time proposals and more accurate forecasts.
2014 - 2015
2014 - 2015
Process Optimization - I led a platform-level FDA application improvement process resulting in a 50% reduction in additional information questions.
2002 - 2014
2009 - 2014
I oversaw a nearly 2X growth in the Division. We maintained top performance in on time delivery of our main deliverable: 510(k) decisions.
2006 - 2009
Technical Evaluation - I presented a complex case to an expert federal panel evaluating Lasik risks, resulting in enhanced safety measures, protecting 1M patients per year. I Initiated a comprehensive evaluation of ophthalmic in-vivo diagnostic devices and developed internal templates for review of complex clinical and engineering issues.
2002 - 2006
Technical Diligence - I have conducted over 1,000 reviews of technologies. Most of my time was spent evaluating cardiovascular pacemaker and defibrillator leads reviews for entire medical device industry, while maintaining workload 2.5 times organizational average. I Collaborated with large cardiovascular companies in developing preclinical techniques for major guidance on evaluation of cardiovascular devices.