PRACTICE
FDA
Overview
PierFerd’s Food and Drug Administration (FDA) practice group regularly provides comprehensive legal services to clients navigating the regulatory landscape of the U.S. FDA. Our FDA Team offers strategic counsel and practical solutions to pharmaceutical, biotechnology, medical device, food, dietary supplement, and cosmetic companies.
Our knowledge spans the entire product lifecycle, from initial development and clinical trials to market approval and post-market compliance. We assist clients in preparing and submitting regulatory filings, responding to FDA inquiries, and managing inspections and enforcement actions. Our goal is to help clients achieve regulatory compliance while advancing their business objectives efficiently and effectively.
Experience
In addition to regulatory compliance, PierFerd’s FDA Team provides robust support in areas such as labeling, advertising, and promotional practices, ensuring that our clients' marketing strategies align with FDA requirements. We also offer guidance on emerging issues, such as digital health, personalized medicine, and the evolving regulatory landscape for cannabis-derived products. By staying at the forefront of regulatory developments and maintaining strong relationships with FDA officials, we are well-positioned to advocate for our clients’ interests and provide timely, informed advice.