Data Reduction Systems

Looking for a seamless way to access your open, older, or closed clinical studies? DRS Corporation’s eTMF Archive Viewer brings everything together in one centralized, searchable platform!

Clinical studies are maintained in many different ways over the years—so what happens when you need to research or reactivate a study that was stored in a system that no longer exists? That’s where our eTMF Archive Viewer comes in.
With this feature, sponsors and CROs can:

✅ Archive study folder structures (TMF Reference Model or customized) and make them easily accessible.
✅ Retrieve study data, no matter which software originally stored it.
✅ Quickly search by file names, reference numbers, keywords, or key identifiers.

We’d love to chat and explore how this can help your team. Reach out to us anytime!

With 40 years of TMF Support experience, we’ve seen every kind of study transfer challenge you can imagine - different formats, different platforms, and plenty of tricky mapping issues.

Our IT team knows how to step in, make sense of complex study transfer files, and keep things moving without delays. Add in our full reconciliation and QA support, and you’ve got a partner focused on getting it right the first time.

Struggling with a study transfer? Let’s talk about how we can make it easier and get your team back to what matters most.

🔐 Data Privacy Isn’t Optional - It’s Foundational

In clinical trials, privacy goes far beyond a checkbox. It’s a core responsibility that underpins everything we do. 🛡️

Your electronic Trial Master File (eTMF) doesn’t just organize documents - it safeguards sensitive data, from patient information to critical regulatory records.

At DRS Corporation, we build privacy and security into every layer of our eTMF:
✅ Role-Based Access – The right people see the right information, nothing more.
✅ Regulatory Alignment – Designed to meet standards like GDPR and 21 CFR Part 11.
✅ Complete Audit Trails – Every action tracked for full transparency and accountability.

Because when it comes to clinical data, protection isn’t optional - it’s essential.

💬 How is your team strengthening data privacy in clinical trials?