eClinPro CTMS & eSource
CTMS/ eSource/ eDocs/ Text SMS/ Recruitment Automation/ Integrated Calendar and many more powerful tools for Clinical Research Sites
What is eClinPro CTMS & eSource?
eClinPro CTMS delivers ONE CENTRAL SOLUTION for Sites, Networks, Sponsors, and CROs. More than just a CTMS, it unifies every essential tool in one platformCTMS, eSource, eRegulatory, eDocs, eConsent, ePay, SMS Text, Recruitment Automation, and Website Integrationwhile also providing EDC, eVisits, eTMF, SDV, Inventory Management, and advanced Reporting. Designed by experienced CRCs, CRAs, Managers, and PIs, eClinPro streamlines workflows across all stakeholders, ensuring seamless collaboration, transparency, and compliance with FDA and ICH regulations. From patient recruitment and pre-screening to study conduct, monitoring, data verification, and final closeout, eClinPro centralizes the entire research lifecycle. Affordable, scalable, and Part 11 compliant, it empowers Sites to manage studies efficiently, Sponsors to maintain oversight, and CROs to monitor trials remotelymaking clinical research faster, simpler, and more reliable.
Screenshots
Video
Features
21 CFR Part 11 Compliance
Audit Trail
Data Capture and Transfer
Data Import/Export
Document Management
Electronic Data Capture
HIPAA Compliant
Patient Monitoring
Workflow Management
Clinical Study Management
CRF Tracking
Forms Management
Third-Party Integrations
FAQ
The official website of eClinPro CTMS & eSource is https://www.eclinpro.com/
eClinPro CTMS delivers ONE CENTRAL SOLUTION for Sites, Networks, Sponsors, and CROs. More than just a CTMS, it unifies every essential tool in one platformCTMS, eSource, eRegulatory, eDocs, eConsent, ePay, SMS Text, Recruitment Automation, and Website Integrationwhile also providing EDC, eVisits, eTMF, SDV, Inventory Management, and advanced Reporting. Designed by experienced CRCs, CRAs, Managers, and PIs, eClinPro streamlines workflows across all stakeholders, ensuring seamless collaboration, transparency, and compliance with FDA and ICH regulations. From patient recruitment and pre-screening to study conduct, monitoring, data verification, and final closeout, eClinPro centralizes the entire research lifecycle. Affordable, scalable, and Part 11 compliant, it empowers Sites to manage studies efficiently, Sponsors to maintain oversight, and CROs to monitor trials remotelymaking clinical research faster, simpler, and more reliable.
eClinPro CTMS & eSource belongs to the Clinical Trial Management, Electronic Data Capture category.
eClinPro CTMS & eSource offers features such as 21 CFR Part 11 Compliance, Audit Trail, Data Capture and Transfer, Data Import/Export, Document Management, Electronic Data Capture, HIPAA Compliant, Patient Monitoring, Workflow Management, Clinical Study Management, CRF Tracking, Forms Management, Third-Party Integrations.
No, eClinPro CTMS & eSource does not offer a free trial.
Pricing
Starting at:
$150/per month
Free Trial Available