Your Journey to AI Accelerated Clinical Research Begins Here
Partners
Together, we accelerate trials, expand impact, and transform what’s possible in clinical research.
CTMS, EDC, eTMF, eConsent, and RWE platforms that power the modern research stack—Trialynx connects seamlessly through structured, digital-ready outputs.
Experts are the brains of clinical trials; we partner with medical writers, project managers, and regulatory experts to deliver better trials, faster.
We move faster together. Our enablement partners help configure, deploy, and scale Trialynx inside real-world research environments—so teams adopt faster, deliver sooner, and see results immediately.
IRB review doesn’t have to slow things down. We work with IRB experts and ethics consultants to align documentation from the start—accelerating approval timelines and reducing back-and-forth
"It's with mixed feelings that I found Trialynx. It makes building studies and writing documents effortless. I wish I'd had it earlier; it would've saved me countless hours."
"Working with Trialynx is a game changer. We completed 40 fully customized protocols—each turned around in just 48 hours—enabling us to launch all of our trials weeks ahead of schedule."
Expert services + powerful technology = smarter research.
Whether you need a turnkey trial development service or want to empower your internal teams with intelligent tools, Trialynx meets you where you are.