Conference: RAPS Convergence 2026
Date: September 15 - 17, 2026
Location: Charlotte Convention Center, Charlotte, North Carolina
Booth: 1019
Aligning science, regulation, and strategy — for 50 years and what comes next
RAPS Convergence turns 50 in Charlotte, and the regulatory profession has never faced a faster-moving landscape. Meet Certara at Booth 1019 to see how expert strategy and purpose-built technology help you navigate AI regulation, global submissions, and evolving health-authority expectations — so you can bring safe, effective products to patients, sooner.
RAPS exists to develop a competent global regulatory workforce that advances public health — a mission Certara shares. This year’s Convergence puts a spotlight on the forces reshaping regulatory affairs: generative AI and its oversight, increasingly complex global submission strategies, digital health, and the growing demand to align science, regulation, and business strategy. Certara meets those challenges with seasoned regulatory strategists and technology built for the way regulatory teams actually work. Stop by Booth 1019 to talk through your submission goals with the people and tools behind them.
How Certara supports your regulatory journey
From strategy to submission, we connect the dots the Convergence agenda is built around.
Set the strategy: Global Regulatory Strategy Consulting
Certara’s Global Regulatory Strategy Consulting team integrates regulatory intelligence into your development strategy, translating global frameworks — FDA, EMA, MHRA, PMDA, and beyond — into actionable local plans. From orphan and accelerated pathways to lifecycle management, our consultants help you reach regulatory milestones with confidence. The same team provides regulatory authoring and content-development support — from FDA and EMA meeting requests and briefing books to eCTD module summaries — delivered as an integrated part of your regulatory strategy. Learn more
Write with human-at-the-helm AI: CoAuthor™
CoAuthor is Certara’s GenAI software for regulatory and medical writing. Built by writers, for writers, it pairs a purpose-built biomedical GPT with an eCTD template library and structured content authoring — right inside Microsoft Word — so teams draft consistent, compliant documents faster while keeping a human in the loop. It’s a working answer to the conference’s central question of how to adopt AI responsibly. Learn more
Get to submission faster: GlobalSubmit™
GlobalSubmit is Certara’s eCTD software to publish, validate, review, and transmit submissions — eliminating risk and expediting regulatory acceptances. As global submission strategy grows more complex, GlobalSubmit keeps your dossiers compliant and submission-ready across regions. Learn more
Digital Resources from Certara
Explore best practices in regulatory strategy, submissions, and AI-enabled writing before you arrive.
Book a meeting
FAQs
Where can I find Certara at RAPS Convergence 2026?
We’ll be at Booth 1019 at the Charlotte Convention Center, September 15–17, 2026. Stop by or book a meeting in advance using the form above.
What will Certara be showcasing this year?
Our focus is the full arc from strategy to submission: Global Regulatory Strategy Consulting, GlobalSubmit™ eCTD software, and CoAuthor™, our GenAI regulatory and medical writing platform.
How does Certara approach AI in regulatory writing?
CoAuthor™ uses a purpose-built biomedical GPT with a human-at-the-helm approach, keeping writers in control while accelerating drafting, quality control, and consistency across documents.
Does Certara provide regulatory writing services?
Yes, as part of our regulatory strategy engagements. Certara’s regulatory experts provide authoring and content-development support, including FDA and EMA meeting requests, briefing books, and eCTD module content and summaries. Our CoAuthor™ software enables AI-assisted, human-at-the-helm drafting of regulatory and medical documents.
What we do not offer is standalone medical writing as a separate service. Our content-development support does not include submission publishing, formatting, hyperlinking, or QC — GlobalSubmit™ handles the publishing and validation side.
Can I schedule a dedicated meeting before the event?
Yes. Complete the meeting form on this page and a member of our team will follow up to lock in a time at the booth.
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