RCCB provides FDA and international regulatory advice and guidance to early stage through more mature companies in the medical device, pharmaceutical, cosmetic, food product, additive manufacturing, and life sciences industries through every stage of the business and product lifecycle. We advise on regulatory strategy, product development requirements and documentation, quality and compliance systems (including FDA, ISO, and cGMP frameworks), site registrations, audits, and commercialization readiness. Our approach is integrated with corporate and transactional counsel, helping clients align regulatory compliance with product development, strategic partnerships, financing, M&A activity, and market expansion. Utilizing business and legal experience in managing FDA-regulated businesses, the practice delivers practical, business-focused guidance that helps clients bring products to market efficiently while managing regulatory risk and supporting long-term growth.
