Local regulatory expertise (eCTD 4.0 readiness), submission / project management with sizeable and scalable global delivery centers
Regulatory Submission Services
Optimize business processes across the regulatory value chain.
DXC’s teams of regulatory submission experts will ensure that your life sciences organization achieves fully efficient, end-to-end submission processes. Your business will maintain compliance with country or regional regulations in multiple markets, covering document formatting, document publishing, dossier publishing, submission filing and archiving.
We provide flexible and extensive electronic Common Technical Document (eCTD) capabilities the FDA / EMEA and other agencies worldwide. DXC can tailor our service options and solution models to support clients’ individual needs.
Local regulatory expertise (eCTD 4.0 readiness), submission / project management with sizeable and scalable global delivery centers
Blended pricing models that leverage offshore centers to allow 20-30% savings versus internal operations
A team of experienced and long tenured publishers, submission managers and regulatory operations subject matter experts
Proven business continuity and disaster recovery methodologies, with a globally distributed delivery model that facilitates a flexible and scalable continuous workflow for clients.
Various service options and flexible solution models that can be tailored to support clients’ needs
Increased cost savings and convenience by eliminating the need to maintain large internal groups to handle traditional spikes in work
Life sciences companies can speed regulatory approval with Gen AI
Harnessing AI to revolutionize healthcare
Leveraging technology supports health equity