Overview
We conduct due diligence reviews for Food and Drug Administration (FDA)-regulated companies engaging in mergers, acquisitions, licensing deals, and other corporate transactions. Our team is able to readily identify and evaluate the significance of FDA regulatory issues that may affect the value of a proposed transaction. Our firm knowledge of all junctures of FDA regulation enables us to incorporate regulatory diligence findings thoroughly into deal negotiations and terms. We also work closely with our corporate partners to identify other corporate issues that may have bearing on the overall negotiations.
Contact Us
Ann M. Begley
202.719.4585 | abegley@wiley.law
Ryan Michael Fournier
202.719.7389 | rfournier@wiley.law
Related Capabilities
- Drug Product Development and Approval Strategies
- Due Diligence and Transactional Support
- Enforcement & Recalls
- Hatch-Waxman Act Litigation
- Human and Animal Food Ingredient Review and Approval Strategies
- Labeling, Advertising, and Promotion
- Litigation and Administrative Advocacy
- Medical Devices
- Regulatory Compliance
- White Collar Defense & Government Investigations