Edgar J. Asebey

Partner @Frier Levitt

Fort Lauderdale, FL, US

I am a partner in the Life Sciences Practice Group of Frier Levitt. As a life sciences regulatory and transactional attorney, I advise pharmaceutical, biotechnology, biologics, medical device, food, and dietary supplement companies on FDA compliance and related regulatory matters, including licensing, transactions, and venture finance.I also represent clients before the U.S. Food and Drug Administration (FDA), the United States Department of Agriculture (USDA), U.S. Customs and Border Protection (CBP), the U.S. Federal Trade Commission (FTC), the U.S. Environmental Protection Agency (EPA), the National Institute for Occupational Safety & Health (NIOSH), and the Drug Enforcement Agency (DEA). My work includes providing compliance and enforcement defense services before these agencies. I assist companies with FDA registration, clearance, and pre-market approval, and advises on compliance throughout the development, manufacturing, marketing, and sale of FDA-regulated products.I also conduct regulatory due diligence to support venture financings, public offerings, and M&A transactions, and advises emerging life sciences and psychedelic drug development companies on patent strategy, FDA regulatory pathways, and clinical trial planning. Since 2016, I have counseled cannabis and hemp businesses, providing regulatory, transactional, and due diligence services to hemp/CBD, cannabis/marijuana, and psychedelics biotechnology companies.

University of Chicago

Bachelor of Arts (BA), Biology

The Catholic University of America, Columbus School of Law

J.D., Law