McKenzie Cato's expertise is assisting medical device, pharmaceutical, and other life science industry companies with pre- and post-market FDA regulatory topics. McKenzie helps companies in developing their regulatory strategy, preparing regulatory submissions, responding to FDA requests for information and data, drafting regulatory policies and procedures, and reviewing advertising and promotional materials. McKenzie also assists companies with FDA, DOJ, and DEA enforcement matters, regulatory due diligence, and state regulatory and licensing issues.

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