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EMWA Spring Conference 2025

May 6-9,2025
Riga, Latvia

Event: EMWA Spring Conference 2025

Date: May 6-9,2025

Location: Radisson Blu Latvija Conference&Spa Hotel,Riga,Latvia

The European Medical Writers Association was founded in 1989 by a small group of professional biomedical communicators with academic, industrial and journalistic affiliations. EMWA has grown since then and now has over 1,000 members from 39 different countries (including 12 countries outside Europe) and includes academics and professionals working in-house or freelance for pharmaceutical and medical communications companies, research institutes, and in the field of scientific journalism.
AlphaLife Sciences is excited to participate and share our insights at the event. We look forward to engaging with you in person!


Booth Number: TBD


Presentation from AlphaLife Sciences:

Date: May 7

Time:  TBD

Speaker: Mike Liang, Head of AI Product & Strategy, AlphaLife Sciences

Session type: Lunchtime seminar

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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