Donna-Bea Tillman

Donna-Bea Tillman is a Principal Consultant at Biologics Consulting with extensive experience in the medical device regulatory field.1 She is a biomedical engineer who has spent over two decades working in medical device regulation, including a significant 17-year tenure at the U.S. Food and Drug Administration (FDA).1 Her background combines technical expertise in biomedical engineering with in-depth knowledge of regulatory processes, making her a valuable asset in the biologics consulting industry.

Professional Experience

FDA Career:: Donna-Bea's 17 years at the FDA have provided her with insider knowledge of regulatory procedures and requirements, which is highly beneficial in her current consulting role.1

Industry Expertise:: With more than 20 years of experience in medical device regulation, she has developed a comprehensive understanding of the field's complexities and evolving landscape.1

Current Role

As a Principal Consultant at Biologics Consulting, Donna-Bea likely leverages her extensive background to assist clients in navigating the regulatory pathways for medical devices and biologics. Her unique combination of engineering knowledge and regulatory experience positions her as a valuable resource for companies seeking guidance in bringing their products to market.