Modern Clinical Data Management
for Teams Moving Faster.
Meet us at Booth 516 + 518
OpenClinica helps sponsors, CROs, and clinical data teams streamline study startup, improve data quality, and simplify trial operations with unified EDC, eConsent, eCOA, and data management workflows — without the complexity of traditional enterprise systems.
Here’s what changes when your eClinical stack actually fits your team.
Build studies with real-time validation and CDASH-aligned templates. Your sites enter it right the first time.
Drag-and-drop study builder, pre-built CRF templates, and a dedicated CSM who’s onboarded hundreds of studies.
Every client gets a named Customer Success Manager — not a ticket queue — who knows your study, your team, and your goals.
An intuitive interface means less training, fewer support calls, and coordinators who don’t dread data entry.
Pull labs, meds, and vitals directly from source systems. Save coordinators hours per patient and cut transcription errors at the source.
Precision-targeted recruitment with real-time analytics delivers 3–5× lower cost per conversion.
SCDM only happens once a year.
Make the 30 minutes count.
Whether you’re evaluating EDC options, trying to cut study startup timelines, or figuring out how to reduce the operational load on your data team — our team is here to help. No pitch decks. Just a real conversation about what you’re working on.
- Evaluating EDC or switching from your current system
- Running studies across multiple sites and struggling with data quality
- A sponsor or CRO exploring eClinical platform options
- A CRO managing studies for multiple sponsors on different platforms
- Thinking about standardizing your eClinical stack
- Running into scale or efficiency problems as your portfolio grows
- A clinical ops or CDM leader thinking about a platform shift
- Dealing with a study startup that’s running behind
- Making a build vs. buy vs. replace decision and want a frank conversation
One platform for the whole study — use what you need, add more when you’re ready.
OpenClinica is modular: start with EDC, layer in eConsent, eCOA, randomization, or recruitment as your studies require.
Build studies in hours with drag-and-drop tools, templated CRFs, and real-time validation. 50% fewer queries.
Learn More →Multimedia consent with comprehension checks, secure e-signatures, and automated re-consent — remote, in-person, or hybrid.
Learn More →Mobile-friendly patient-reported outcomes with automated reminders. Increase compliance, reduce missing data.
Learn More →Simple to complex schemes — blinded/unblinded access, inventory management, automated notifications — integrated with study data.
Learn More →Pull lab results, medications, and vitals from EHR systems directly into your EDC. Hours saved per patient. Transcription errors eliminated.
Learn More →Real-time dashboards for enrollment tracking, query management, and site performance. Customizable for every stakeholder.
Learn More →Precision-targeted outreach with smart pre-screening and real-time analytics. 3–5× lower cost per conversion.
Learn More →| You Build It | We Build It For You |
|---|---|
| ✓Drag-and-drop study builder | ✓Experienced study build consultants |
| ✓Pre-built CDASH CRF templates | ✓Full-service CRF design and setup |
| ✓On-demand training via LMS | ✓Protocol review and recommendations |
| ✓24/5 application support | ✓Validation documentation included |
What clinical data teams say after switching.
After 15 years as a customer, we can confidently say that OpenClinica continues to earn our trust. Their EDC has supported a range of projects for us, including pediatric studies, early-phase safety work, later-phase evaluations, and research aimed at enhancing gut health.
If not for OpenClinica and your team and your abilities, we would not be saving lives. We would not be able to reach the people who need it the most — the people who are literally hidden in the system and that are not seen.
Stop by — we’ll show you, not tell you.
See live demonstrations of our EDC, eConsent, eCOA, and EHR-to-EDC workflows. If you’re evaluating platforms, 15 minutes at the booth will tell you more than any spec sheet.
- ▶EDC study build: watch a form go from blank to live
- ▶eConsent workflow: end-to-end consent for a hybrid trial
- ▶EHR-to-EDC: a live pull of lab data into the CRF
- ▶Query management dashboard: see how data review actually works
+518
SCDM fills up fast.
Book your slot now.
Our team has limited availability during the conference. Reserve time with Sam, Mark, or Andy before their calendars close — or just show up at Booth 516 + 518.
Contact Our Team → openclinica.com