Event: 2026 DIA Regulatory Submissions, Information, and Document Management Forum
Date: Feb 2-4, 2026
Location: Bethesda North Marriott Hotel and Conference Center
(5701 Marinelli Road, North Bethesda, MD 20852)
The DIA Regulatory Submissions, Information, and Document Management (RSIDM) Forum is a premier platform dedicated to optimizing the operational efficiency of regulatory information to accelerate patient access to therapeutics. By convening industry stakeholders and regulators, the forum examines evolving data standards and integrated approaches to align people, processes, and technology. Attendees gain invaluable insights into building successful RSIDM foundations, adopting innovative technologies, and achieving regulatory excellence through specialized tracks focused on the end-to-end management of high-quality health authority submissions.
Booth Number: 201
Presentation from AlphaLife Sciences:
Date: Feb 2
Time: 10:50 AM-11:20 AM
Speaker: William Chen, Principal Business Solution Architect, AlphaLife Sciences
Topic: How Leading Global Pharma Embraces AI to Automate Regulatory and Medical Documents with Quality Control
We recognize that the foundation of a successful RSIDM strategy lies in the ability to manage complex information with absolute precision. Our AI-powered ecosystem is specifically designed to streamline the end-to-end management of regulatory assets, ensuring high-quality, submission-ready outputs including:
Structured Content Authoring: Accelerating the transition from raw data to compliant Clinical and Regulatory documents.
Regulatory Information Management (RIM) Augmentation: Utilizing AI to harmonize data across disparate systems and evolving standards.
eCTD & Document Automation: Reducing manual overhead in the preparation of global submission dossiers.
Data-to-Document Transformation: Ensuring consistency and traceability from R&D data to final Health Authority filings.
By integrating AlphaLife Sciences’ solutions, organizations can build a resilient RSIDM foundation that not only meets current requirements but is future-proofed for the era of AI-driven regulatory excellence.
To request a meeting, fill out the form provided and a representative will be in contact soon to schedule.
