As a pioneer in electronic
regulatory submissions,
we help streamline your work and raise its quality.
eSA, Inc. supports the pharmaceutical industry’s regulatory and submission work — from automating eCTD creation to publishing and reviewing submission deliverables — through both tools and services.
Miyabira
Grace-driven Regulatory Operations foundation.
From authoring, validating, and publishing submission deliverables to viewing and reviewing eCTDs — a new foundation for regulatory operations.
Learn more →Products
From authoring submissions to compiling eCTDs.
We provide a range of tools and solutions for the pharmaceutical industry, including AiX, the eP2AS series, and uniTemplate.
View all products →Services
From eCTD authoring support to consulting.
We provide outsourcing services tailored to your needs, including DMF submission support, on-site support, and consulting.
View all services →About eSA
A pioneer in regulatory submission digitization.
Learn about eSA, Inc.’s history, business, and company information.
Company information →Bring quiet precision to your regulatory and submission work.
Have questions about our products or services, or interested in adoption? We’re happy to hear from you.