About Jessica Ringel

Jessica Ringel advises medical device, pharmaceutical and HCT/P manufacturers and distributors on matters spanning the entire FDA regulatory lifecycle. Jessica’s post-market practice focuses on quality and compliance matters, including responses to FDA inspections and enforcement actions, recalls and adverse events, and advertising and promotion. Her pre-market practice includes advising on regulatory strategy and marketing applications. Jessica’s regulatory practice is complemented by life sciences transactional matters, conducting FDA regulatory due diligence evaluations regulatory compliance history, health and risk, and preparing and negotiating terms and provisions in related agreements.