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DIA 2025 Global Annual Meeting

June 15-19,2025
Washington, DC

Event: DIA 2025 Global Annual Meeting

Date: June 15-19,2025

Location: Walter E. Washington Convention Center801,Allen Y. Lew Place, NW,Washington, DC

DIA 2025 is the ultimate global gathering for industry pioneers, regulatory experts, and healthcare visionaries. This flagship event is more than just a conference—it’s a catalyst for change, bringing together the brightest minds to shape the future of healthcare, drug development, and regulatory science. Through groundbreaking discussions, dynamic networking opportunities, and hands-on learning experiences, DIA 2025 empowers attendees to drive meaningful progress in the life sciences sector.
AlphaLife Sciences is excited to participate and share our insights at the event. We look forward to engaging with you in person!


Booth Number: 1941


Presentation from AlphaLife Sciences:

Placement: Lunch 2

Date: June 16th
Start Time: 12:55 PM
End Time: 1:25 PM

Speaker: Sharon Chen, Founder and CEO, AlphaLife Sciences

Location: Innovation Theater #1

Topic：GenAI in Action: Demo and Real-World Case Studies Automating Document Authoring for Regulatory Submissions and Scientific Reports in Top Global Pharma


This session unveils an off-the-shelf, GenAI-powered platform revolutionizing document authoring for regulatory submissions and scientific reports, already proven in global pharmaceutical deployments. Featuring real-world case studies powered by the AuroraPrime AI platform—a trusted solution used by 5 of the top 10 global pharmaceutical companies and leading CROs—this showcase highlights how AuroraPrime is transforming regulatory and medical writing.

Key benefits include:
  • Significantly reducing first-draft time for CSRs, protocols, and more.
  • Delivering 30–50% overall time savings for CSRs, as validated by two top-ten pharma companies.
Attendees will experience a live demonstration of AuroraPrime’s most impactful AI features, designed to enhance compliance, quality, and consistency. These include:
  • AI-powered templating engine for streamlined document creation.
  • Automated Quality Check to ensure accuracy and adherence to standards.
  • Versioning for seamless document management.
  • Multimodal Data Ingestion for integrating diverse data sources.
  • No-code application for easy adoption and usability.
Discover how forward-thinking teams are accelerating timelines and adopting best practices in clinical document creation. This session offers actionable strategies, real-world insights into AI applications, and measurable success stories, empowering attendees to optimize their document authoring processes.
Join us to explore how AuroraPrime is setting new benchmarks in efficiency, compliance, and innovation for regulatory and scientific writing in the pharmaceutical industry.

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