We have been working on clinical research projects with our clients for the last 19 years, we help them to build eCRFs for every type of study, whether they are either very complicated or super simple, but always obtaining high-quality data and facilitating the data collection process.
- Pharmaceutical Companies
- Medical Device Companies
- Biotechnology Companies
- Research centres
- Medical societies
- Clinical Trial: Phase I,II, III and IV
- Observational Studies
- Patient Registries
- Post-Market Surveillance
- Medical Devices Studies
- Preclinical Studies
- Nutritional Studies
You do not want an eCRF!
What you want is to collect high-quality data for your clinical study safely and avoid the problems associated with this complicated process, and if possible, without ruining you.
The biggest eCRF's problems are: the initial eCRF creation and the mid-study changes, which occur in 97% of the studies. Use ShareCRF and forget these problems.
Take a Free Tour of ShareCRF
- Make Your Own eCRF. No Programming.
- Full Compliance. GCP/EMA/FDA/GDPR/HIPAA.
- Secure Mid-Study Changes. Test Environment.
- Monitoring management. Queries.
- Configurable approval workflow.
- Hosting included. Cloud-Based solution.
- Randomization. Trial Supply Management.
- Multi-device: Desktop, Tablet and SmartPhone.
- Configurable Roles.
- High-Quality Data. The Best "edit check" engine.
- Audit Trail.
- Electronic Signature.
- Export Data when you want. CSV, SPSS, SAS and Excel.
- Data Backup automatically and secured.
- For simple and complex trial.
- Always the last and modern version of ShareCRF.
- Technical Support.
- Quicks changes to adjustments to protocol amendments.
- Easy access for investigator.