Our regulatory staff is experienced and ready to assist you with appropriate regulatory documentation for submissions in the United States, Europe and the rest of the world. They routinely review new regulatory documentation to provide customers with the most up to date information regarding the manufacture of biological products. They also work closely with internal staff to determine what course of action is required to ensure our facility is in compliance with any new regulations. Our staff is experienced in working with customers to assist in resolving questions raised by the FDA and other regulatory agencies worldwide regarding how their products are manufactured at Avid Bioservices.