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BiotechX US 2025

Sep 16-17,2025
Philadelphia,PA

Event: BioTechX USA 2025

Date: Sep 16-17,2025

Location: Hall F Pennsylvania Convention Center, PA

BioTechX USA covers diagnostics, precision medicine and digital transformation in pharmaceutical development and healthcare. Now running for the third year, we are continuing conversations on the East Coast and will both maintain and foster new relations with key stakeholders in the healthcare industry.
Our 2-day event will take place in 2025 in Pennsylvania, a thriving hub of innovation. We are aiming to bring 1500 global executives, 300 speakers, 100 sponsors and exhibitors and 50 start-ups.
AlphaLife Sciences is excited to participate and share our insights at the event. We look forward to engaging with you in person!


Booth Number: 903


Presentation from AlphaLife Sciences:

Date: Sep 16
Start Time: 12:05 PM
End Time: 12:20 PM
Track: AI in Clinical Trials
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 an era where speed, accuracy, and compliance are paramount, leading global pharmaceutical companies are increasingly leveraging artificial intelligence to transform the way regulatory and medical documents are created. This presentation will explore how top pharma organizations are implementing AI-driven solutions to automate the drafting of high-quality clinical and regulatory content — including protocols, CSRs, IBs, and more — while embedding robust quality control mechanisms throughout the workflow. Drawing from real-world case studies, we will highlight best practices for aligning AI tools with internal compliance standards, ensuring traceability, and driving efficiency across cross-functional teams. Attendees will gain insights into how AI can not only accelerate timelines but also enhance consistency, scalability, and collaboration in regulatory and medical writing operations.

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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