Dustin Folio, JD

senior consultant

Dustin Folio has been working in the medical device industry as a Regulatory Affairs Professional for over 6 years. During this time he has worked on Class I, II, and III devices performing both pre-market and post-market activities for companies ranging from small startups to fortune 500 companies. He has helped several companies navigate the complete design control process; providing regulatory support from device conception through regulatory submission and launch, as well as post-market changes, maintenance, and renewals. Dustin has extensive experience with both US and EU MDR regulations, as well as many LATAM, Middle Eastern, and South American geographies, plus Canada and Australia/New Zealand.

Dustin supports the team at Folio Consulting Group, LLC. For more information on their regulatory, quality, and project management services visit their website.