Next-generation eClinical capabilities when you need them
Timaeus provides research organisations critical eClinical advantages from Study Design through Reporting
- Agile trial configuration
- Capture and inline integration of clinical data from any source or location
- Automatic validation checking and medical coding of data from the start
- Real-time monitoring, data management and reporting
- Amendment of trials on-demand, without site interruption
Easy and hassle-free using Timaeus-as-a-Service
Timaeus-as-a-Service (TaaS) rapidly provides eClinical benefits without bogging you down managing technology. We will take care of everything for you:
- Infrastructure provisioning and hosting with 24/7 monitoring and security
- Study start-up, go-live and archive
- Global site assessment, initiation, archive and support
- Role-based user training with 21 CFR Part 11-compliant sign-off
You only need one trial to start
With TaaS, you benefit from our large-operational efficiencies on your first trial. You do not have to invest in people or technology. Tell us below how we can demonstrate the benefits of Timaeus to you. We look forward to it.
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