To bring the exciting science of cell and gene therapy manufacturing to life, creating smaller-scale filling solutions is imperative to the success of the ATMP industry. But before you begin scaling your operation, there are important questions to consider about fill-finish in ATMP.
Read MoreTodd Vaughn
Fellow - Aseptic and Sterile Products
Raleigh, North Carolina
Todd Vaughn is a Fellow of Aseptic and Sterile Products in the Southeast region with more than 20 years of experience in process design within the pharmaceuticals industry. His highly technical knowledge and application of industry regulations and CGMPs has made him valuable to his clients in design, commission and qualification of pharmaceutical processes and facilities. Todd is one of our leading technical experts in the areas of aseptic processes, containment of highly hazardous compounds, and regulatory compliance. His focus on patient safety and risk mitigation informs his design strategy helping clients to meet forward thinking goals. He has been key to the growth of the aseptic and sterile filling market at CRB. His involvement in projects include business case feasibility focused on upfront capex decisions through the construction, qualification and startup of the facility.
With his expertise in the design of pharmaceutical fill-finish, sterile processing and highly hazardous compound containment facilities, Todd has utilized his extensive experience and dedication to detail to benefit CRB clients in creating processes and facilities fitting best with their financial and production needs. Described by his colleagues as steadfast and reliable, Todd is known to go the extra mile to provide outstanding client service, always keeping the client’s best interests as his North Star.
Todd is also a dedicated member of the International Society of Pharmaceutical Engineering (ISPE) and Parenteral Drug Association (PDA).