
About company
Suttons Creek partners with pharmaceutical companies, providing consulting services like expert education, guidance and execution for the development, global regulatory approval, and commercialization of their combination product devices and digital support platforms throughout the entire product lifecycle. The complexities of combination product development and regulatory approval are ever-changing. Advancements in science, technology and client-care innovations require constant adjustments by the FDA, the EU MDA and other global regulatory agencies. This is why it is important to have a team of experts who are well- versed in current standards, practices and regulation on your team. When a pharmaceutical company is working to bring a new, life-changing combination product to patients, Suttons Creek and its device and digital support platform specialists bridge the gap between pharma’s medical expertise and the highly specific, varying and intricate world of device regulations.