Dvorah Richman

About

Regulatory attorney with extensive industry and law firm experience focused on FDA medical device laws, regulations and policies. Expertise in a wide range of topics, including imaging devices, in vitro diagnostics, artificial intelligence, product promotion, investigational studies, privacy, FDA enforcement and fraud and abuse. Experience includes: drafting corporate policies and procedures; analyzing business plans; commenting on proposed government rules; drafting and negotiating regulatory contract provisions; conducting due diligence for mergers and acquisitions; facilitating product approvals; analyzing proposed legislation; managing crises; drafting administrative litigation briefs; and providing corporate training about diverse regulatory, compliance and legal topics.