Mark Smutka

Consultant, Regulatory Affairs at InterVene

Mark Smutka is a highly experienced RA/CA/QA Consultant with a strong background in medical device companies. Mark has held various senior-level positions in clinical and regulatory affairs spanning over several decades. Mark has worked with technologies such as interventional cardiology, electrophysiology, orthopedic, and treatments for obesity. Their expertise and knowledge in the field make him a valuable asset to any company Mark consults for.

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