The eSubmissions Solution Accelerator enables the delivery of Adobe LiveCycle applications that manage the development of content for electronic regulatory submissions for life sciences. The accelerator supports the implementation of auditable review, commenting, and approval workflows that leverage the interactive PDF commenting and signature tools in Adobe Acrobat and Reader in conjunction with the workflow management and audit capabilities of Adobe LiveCycle ES.
Other benefits of the accelerator include the ability to leverage server managed PDF generation, direct integration with electronic content management (ECM) systems, version control, and digital signatures (including SAFE BioPharma signatures). By using the accelerator, Adobe partners, system integrators, professional services and customers can deliver LiveCycle applications that let business users easily define structured multi-step, multi-stage review and approval workflow templates that simplify the implementation of SOP-driven regulatory processes for life sciences.

The eSubmissions Solution Accelerator is built on the new Review, Commenting, and Approval and On-Demand Assembly building-blocks, and includes industry- and regulatory-specific samples and documentation. The Review, Commenting, and Approval and On-Demand Assembly building blocks are re-usable technology components that can be used to provide similar auditable review and approval functionality to LiveCycle applications beyond life sciences. They can be used to support processes such as: manufacturing design reviews, legal & policy document reviews, and correspondence review. The eSubmissions Solution Accelerator also includes the updated version of the On-Demand Assembly building block that enables the dynamic, workflow-driven assembly of forms and documents.