DXC's program management services include the management, governance and project coordination to provide the necessary stewardship of the regulatory process.
Getting a drug approved involves coordinating a tremendous amount of information and many people in an ever-shifting regulatory landscape. Life sciences companies across the globe are increasingly turning to managed service providers to help get the job done. DXC provides a full range of global regulatory submission solutions and has the expertise, experience and leadership to guide the complicated process.
DXC's program management services include the management, governance and project coordination to provide the necessary stewardship of the regulatory process. They are an all-encompassing offering designed to ensure smooth workflows, effective communication and, most of all, compliance and quality.
With nearly 25 years of experience managing regulatory submissions, DXC provides extensive subject matter expertise at the project level. With a focus on delivering quality, program management is an integral part of our regulatory submission offerings, and we can tailor management levels to meet your specific needs.
DXC combines a local approach of providing one point of contact located in the same time zone as our clients, along with our massive global reach, which encompasses regulatory submission expertise at all major agencies. Our program management staff includes a healthy balance of industry professionals and consulting professionals, backed by cost-efficient support at offshore locations.