RAPS Convergence 2025

Oct 7-9,2025
Pittsburgh, PA

RAPS convergence

Event: RAPS Convergence 2025

Date: Oct 7-9,2025

Location: David L. Lawrence Convention Center,Pittsburgh

RAPS Convergence 2025, taking place October 7–9 in Pittsburgh, is the premier annual event for regulatory affairs professionals worldwide. Organized by the Regulatory Affairs Professionals Society (RAPS), it brings together leaders from pharma, biotech, medical devices, CROs, academia, and regulatory agencies. With over 150 sessions and workshops, the conference covers the full regulatory lifecycle, offering practical insights, best practices, and global perspectives. Attendees can also earn Continuing Education credits while expanding their professional networks. Whether you are an experienced expert or new to the field, RAPS Convergence is the must-attend event to stay ahead in the regulatory landscape.
AlphaLife Sciences is excited to participate and share our insights at the event. We look forward to engaging with you in person!


Booth Number: 411


Presentation from AlphaLife Sciences:

Date: Oct 8
Chair Session: 12:30 PM-12:55 PM
Exhibit Hall: Discover Theater - 425
Speaker: Sharon Chen, Founder and CEO, AlphaLife Sciences
Topic:  How Leading Global Pharma Embraces AI to Automate Regulatory and Medical Documents with Quality Control
   In today’s regulatory landscape, where compliance, accuracy, and speed are equally critical, global pharmaceutical leaders are turning to artificial intelligence to modernize regulatory and medical writing. This session will showcase how AI-driven platforms are being applied to generate key documents such as protocols, CSRs, and IBs, while embedding rigorous quality control and traceability into every stage of the process. Through practical case studies, we will discuss strategies for aligning AI adoption with internal compliance frameworks and global regulatory expectations. Attendees will learn how leading organizations are using AI to reduce timelines, improve document consistency, and strengthen cross-functional collaboration—ultimately redefining best practices in regulatory writing.
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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