A Modern eClinical Suite for
Tomorrow’s Digital Era
Tomorrow’s Digital Era
Accelerate Your Research with a Fully Integrated & Customizable Platform
How CIMS Can Accelerate Your Research
CIMS eClinical Suite is a cloud-based, fully-validated 21CFR11 compliant intelligent platform. Access comprehensive EDC modules connected to smart mobile apps to streamline the clinical trial process from study setup to regulatory submission.
The full eClinical era is almost upon us, but there’s no need to wait. CIMS can accelerate your research and reduce your costs … today!
CROs
- Bring biostatistics and data management in-house with the full support of our suite and team
- Build databases and eCRFs with point and click
- Increase remote monitoring to reduce CRA cost
- Add FDA access to eliminate site inspections
- Eliminate the need for separate EDC, drug supply and document management systems
- Have real-time access to study progress via our integrated mobile app
Sponsors
- Gain full visibility into your study details – # of patients enrolled, progress, SAEs – right from your mobile device
- Reduce your EDC study cost
- Eliminate the need for separate FDA reporting
- Have an alternative option to being trapped by the expensive market leaders
Post-marketing Studies
- Replace your expensive, high-end system for your post marketing study
- Easily collect data with our fully-integrated mobile system
- Complete a quick study within budget
Investigator Initiated Studies
- Use as an alternative to expensive CRO-managed studies
- Have a single platform for your eTMF, document management, EDC and drug supply
- Gain peace of mind with the full support of our team
University Research
- Switch from Redcat to a fully validated, 21CFR11 compliant intelligent platform for your study
- Eliminate the need to hire a CRO
- Accelerate your research
