Richard Hines is a seasoned professional in regulatory affairs with extensive experience across various medical device companies. Currently serving as Senior Manager of Regulatory Affairs at ImpediMed since August 2022 and Manager of Regulatory Affairs at Zest Dental Solutions since October 2021, Richard specializes in regulatory strategy for new product development, 510(k) submissions, and EU MDR technical file remediation. Previous roles include Senior Manager of Regulatory Affairs at pfm medical, inc., and Regulatory Affairs Manager at BioFilm Inc., where Richard managed regulatory tasks for the USA and Canada, developed global regulatory strategies, and oversaw compliance programs. Richard's experience also encompasses international submissions and regulatory guidance, having worked with companies such as Volcano Corporation and DJO, LLC. Richard holds an education background from San Diego City College.
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