About

Headquartered in Philadelphia, PA, with a satellite office in San Diego, CA, GlobalSubmit is dedicated to facilitating electronic regulatory submissions between life science companies and regulatory agencies worldwide. In addition to developing eCTD software platforms, we provide a host of electronic publishing services, eCTD outsourcing, regulatory consulting and technical support. Since 2005, GlobalSubmit has been the sole eCTD software provider to the U.S. Food & Drug Administration. The FDA relies exclusively on GlobalSubmit’s REVIEW and VALIDATE platforms to evaluate the technical validity of 100% of the electronic submissions it receives.