Manage trial documents efficiently and be inspection-ready at any time with oomnia eTMF

Are you a pharmaceutical company, CRO, academic researcher, or medical device manufacturer looking to streamline your clinical trials? We understand that managing clinical trials can be complex, including keeping trial documents organized and inspection ready. Our solution is designed to help you manage documents efficiently and maintain top quality across all your clinical trials.

What makes us unique?

oomnia is not just another document management tool. You can use eTMF as a stand-alone tool or unlock its full potential as part of our comprehensive platform, allowing your team to focus on research, not paperwork.

How can we help you?

Streamlined Documentation: Reduce the need for multiple logins by accessing eTMF, EDC, RTSM, and CTMS from one platform.
Efficient Administration: Simplify document handling with digitized processes, automated indexing, and easy search functions.
Inspection Readiness: Stay prepared for audits with quick access, standardized filing, and versatile export options.
Secure Access: Ensure data integrity with role-based access, encryption, and regular audits.
Regulatory Compliance: Meet GCP, EMA, ICH guidelines, and CDISC TMF standards effortlessly.

Why trust Wemedoo?

Our clients experience better trial outcomes, lower costs, and seamless document management. Here’s what they say:

"Their dedication and support have been key to our success." — Volodymyr Stus, MD, Polpharma SA
"Always a pleasure to work with Wemedoo’s innovative and detail-oriented team." — Dr. Georg Mathis, CEO, Appletree CI Group AG

Let’s work together

Ready to improve your document management with Wemedoo oomnia eTMF? Click 'Get it now' or book a demo to start your journey with us.

The next step in advancing your clinical research begins here.

Wemedoo oomnia eTMFWemedoo AG

Wemedoo oomnia eTMF

Wemedoo AG

Wemedoo oomnia eTMF

Wemedoo AG

Wemedoo oomnia eTMF
Wemedoo AG