Tonya Morris has worked in the medical device and pharmaceutical industries for over 30 years. She is an experienced scientist and a subject matter expert in many fields of testing, including surface disinfection, filtration sterilization validations, aseptic processing, product microbial activity (potency and preservatives), particulate analysis, container closure systems, contact lens regimen tests, test development, failure investigations, and pharmaceutical product assessments. Her primary tenure has been with Nelson Laboratories LLC where she started in bioburden and radiation sterilization. She participates on the Parenteral Drug Association (PDA), is a co-chair for AAMI/ISO WG9, an executive board member for HCPA, and participates on several Kilmer committees. She enjoys partnering with sponsors to develop test methods, consult, assist with product design, review process controls, and problem-solve.
