Document Level Publishing

Delivering best-in-class regulatory document development and submission services.

Document Level Publishing

Let our expert team help create submission-ready documents that align with regulatory agency specifications. We offer this service for documents authored by Acumen as well as those authored by our clients.

Document level-publishing includes:

  • Formatting of Words documents (styles, cross-references, tables, pagination, etc) to align with agency standards for easy conversion to PDF

  • PDF processing, including QC of all bookmarks, links, and document properties to meet specifications

Submission-level Publishing

Submission-level publishing includes eCTD placement and cross-document linking. We work alongside our trusted partner WAYS Pharmaceutical Services, a company with unsurpassed knowledge and skill in managing all aspects of submission publishing.

WAYS has experience with all application types, including INDs, NDAs, BLAs, ANDAs, DMFs, and Orphan Drug Applications and can ensure your fillings are eCTD compliant.

If you have an upcoming submissions, consider WAYS as your go-to publishing experts. Our teams have collaborated on many successful submissions, and together we provide a client-focused, integrated end-to-end submission team.

Click here to connect with WAYS.