The RAPS Project Management Collaborative Community is dedicated to discussing various aspects of regulatory project management. This includes the role of the regulatory project manager, collaboration with regulatory specialists, and influencing drug development decisions. Additional topics of interest may encompass Project and Submission Management Artifacts (Tools) for Regulatory Affairs, such as the use of submission planning features within Veeva RIM compared to MS Project, Smartsheet, and others. Furthermore, discussions may also cover Documentation Management Systems, including comparisons between Veeva and SharePoint.