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Conference: AMWA Carolinas 2025 Spring Conference

Date: May 16, 2025

Location: Friday Center, Chapel Hill, NC

At Certara, we accelerate medicines to patients, partnering with life science innovators. Together we advance modern drug development with biosimulation, regulatory science, and market access solutions. We use software, technology, and services to transform traditional drug discovery and development. Our clients include more than 2,400 biopharmaceutical companies, academic institutions, and regulatory agencies across 70 countries.

Hear insights from Certara experts

Morning Session
Resume Review

Laura Sheppard, Sr. Director, Regional Head Clinical Regulatory Writing

Laura will be at AMWA Carolinas to provide resume reviews and connect with candidates in person, offering her expert guidance to help you take the next step in your career. Don’t miss this chance to engage directly with a leader transforming our industry. Laura Sheppard, Regional Head for Clinical Regulatory Writing for North America, Head of Lay Language Writing, and Head of Strategic Relationship Management

Afternoon Educational Session
Track A: The Good and the Bad: Clinical Disclosure

Demetrius Carter. SVP, Regulatory Sciences & Medical Affairs

The Declaration of Helsinki set the standard for ethics in human research, making transparency central to medical progress. While regulators like the ICH, FDA, and EMA have built on that, inconsistent reporting still challenges trust and patient safety. At Certara, we’re committed to changing that. Join Demetrius as he shares how we’re driving transparency in drug development—so every patient benefits from innovation. Demetrius Carter, SVP, Regulatory Sciences & Medical Affairs, Certara, Inc

On time, every time: Expert regulatory writers and CoAuthor™ GenAI technology delivering successful submissions faster.

Resources

From molecule to market, Certara is your trusted partner in the drug development journey. Backed by a team of experts and innovative technology, we’re here to guide and support you at every stage. Explore our expertly curated resources, and feel free to reach out with any questions.

AI Enabled Regulatory Writing

Initial Clinical Trial Application:

Mid-Stage Development

Post Marketing

Medical Writing