The new cleanroom at our global headquarters in Salt Lake City, Utah, was designed for today's rigorous contamination control expectations, driven by EU GMP Annex 1. Learn More
Katrina (Katy) Hurst is an expert in biocompatibility, especially with respect to the relationship between medical device materials, biological systems, and the analytical procedures used to evaluate biocompatibility in vitro and in vivo. Katy has extensive expertise in writing biological...
Susan has over 40 years of quality-assurance experience in the pharmaceutical industry. She has earned several awards from the Parenteral Drug Association (PDA), including Distinguished Author Award, Distinguished Service Award, and Gordon Personeus Award. Serving as a volunteer in a...
Jordan has 15 years of experience navigating regulatory pathways and identifying optimal regulatory strategies for pharmaceutical and medical device companies. As Director of Regulatory Affairs for Regulatory Compliance Associates (RCA) he is responsible for providing clients with general direction, tactical...
Griffin Cammack has worked at Nelson Labs for over 8 years, specializing in cleaning, disinfection, and sterilization validations of reusable medical devices. His current role as Expert Technical Consultant at Nelson Labs involves providing assessments and justifications for reusable medical...
Bryce Telford is a recognized authority and industry leader on radiation sterilization, bioburden, microbiology, and tissue processing. He has over 15 years of experience working in laboratory functions in research, test design, media formulation, medical device, and tissue industries. He...
