---
description: Review of diCELLa eCRF clinical trials Software: system overview, features, price and cost information. Get free demos and compare to similar programs.
image: https://gdm-localsites-assets-gfprod.imgix.net/images/software_advice/og_logo-55146305bbe7b450bea05c18e9be9c9a.png
title: diCELLa eCRF clinical trials | Reviews, Pricing & Demos - SoftwareAdvice GB
---

Breadcrumb: [Home](/) > [Clinical Trial Management Software](/directory/4623/clinical-trial-management/software) > [diCELLa eCRF clinical trials](/software/437239/dicella-ecrf-clinical-trials)

# diCELLa eCRF clinical trials

Canonical: https://www.softwareadvice.co.uk/software/437239/dicella-ecrf-clinical-trials

> diCELLa Unlimited is a tool that enables effective clinical trial management at every stage, from trial design, through data collection and patient safety management, to trial documentation management and monitoring the activities of all parties involved in the clinical trial process.

diCELLa Unlimited has integrated eCRF and CTMS modules.

The application is focused on the needs of the Sponsor/CRO and the research team. 

Our system offers all the necessary modules:
1. eCRF with remote monitoring module
2. CTMS
3. IWRS/RTSM, 
4. SAFETY: AE/SAE Tracking, Safety Management
5. CTMS interated with eCRF
5.a. patients management
5.b. sites management
5.c. SOP development
5.d. Agreements management
5.e. Team activities and working time/trip reporting
6. Query analysis
7. Finances, Budget Management and invoicing
8. eTMF/eISF
9. ePRO
10. Central Imaging Lab.

Key Features:
1. All types of randomization
2. Defined randomization procedures
3. Real-time randomization status tracking
4. Defined procedures for reporting adverse events
5. Management from the level of site, CRO and sponsor
6. Defining IMP management procedures
7. Track deliveries, shipments, allocations, inventory and assignments
8. Management of entities related to the clinical trial
9. The possibility of creating different categories of entities
10. The ability to assign a subcontractor to various projects
11. Knowledge management in the organization
12. All projects in one platform
13. CTMS REAL TIME DATA 100% integration with eCRF
14. Overview of all clinical trials at the site, quick access to trial results in the specific site
15. List of all patients from all sites in the clinical trial
16. Analysis of the completion status in the eCRF
17. Recruitment progress statistics
18. Query response analysis
19. SOP management
20. Remote monitoring.
> 
> Verdict: Rated \*\*\*\* by 0 users. Top-rated for **Overall Quality**.

-----

## About the vendor

- **Company**: diCELLa

## Commercial Context

- **Starting Price**: €15,000.00
- **Pricing model**: Flat Rate (Free Trial)
- **Pricing Details**: 1. Customized Quotation: We provide a tailored quote based on your submission form.

2. Flexible Pricing: Our configuration costs are designed to fit your needs, depending on the complexity of your clinical trial, the number of visits, patients, and centers involved.

3. Transparent Estimates: We promptly send you a detailed quote for your review.

4. Seamless Onboarding: Once you accept our financial terms and sign the contract, simply provide us with your protocol and/or preliminary CRF.

5. Swift Setup: In just 5 days, we will prepare a customized eCRF for you.

6. Collaborative Customization: Engage in a collaborative process with us to fine-tune and align the eCRF with your workflow, ensuring it meets your team's unique needs.

7. Reliable Validation: Upon your approval, we conduct thorough validation, making sure your eCRF is ready to collect data seamlessly.
8. Ongoing Support: After the eCRF goes live, benefit from our continuous support with a straightforward monthly fee.
- **Target Audience**: 11–50, 51–200, 201–500
- **Deployment & Platforms**: Cloud, SaaS, Web-based
- **Supported Languages**: English, Polish
- **Available Countries**: Czechia, Italy, Poland, Romania, Russia, Slovakia, Spain, Switzerland

## Features

- 21 CFR Part 11 Compliance
- API
- Access Controls/Permissions
- Activity Dashboard
- Activity Tracking
- Ad hoc Reporting
- Alerts/Notifications
- Audit Management
- Audit Trail
- CRF Tracking
- Clinical Study Management
- Compliance Management
- Customisable Forms
- Customisable Reports
- Data Capture and Transfer
- Data Import/Export
- Data Synchronisation
- Data Verification
- Data Visualisation
- Digital Signature

## Support Options

- Email/Help Desk
- FAQs/Forum
- Phone Support
- 24/7 (Live rep)

## Category

- [Clinical Trial Management Software](https://www.softwareadvice.co.uk/directory/4623/clinical-trial-management/software)

## Alternatives

1. [Florence eBinders](https://www.softwareadvice.co.uk/software/371223/ebinders) — 4.5/5 (83 reviews)
2. [Castor EDC](https://www.softwareadvice.co.uk/software/109506/castor-edc) — 4.7/5 (204 reviews)
3. [Researchmanager – Clinical Research Suite](https://www.softwareadvice.co.uk/software/108609/research-manager) — 4.2/5 (112 reviews)
4. [ShareCRF](https://www.softwareadvice.co.uk/software/357170/sharecrf) — 4.8/5 (44 reviews)
5. [Jeeva eClinical Cloud](https://www.softwareadvice.co.uk/software/267792/jeeva-eclinical-cloud) — 4.8/5 (12 reviews)

## Links

- [View on SoftwareAdvice](https://www.softwareadvice.co.uk/software/437239/dicella-ecrf-clinical-trials)

## This page is available in the following languages

| Locale | URL |
| en | <https://www.softwareadvice.com/clinical-trial-management/dicella-ecrf-clinical-trials-profile/> |
| en-AU | <https://www.softwareadvice.com.au/software/437239/dicella-ecrf-clinical-trials> |
| en-GB | <https://www.softwareadvice.co.uk/software/437239/dicella-ecrf-clinical-trials> |
| en-IE | <https://www.softwareadvice.ie/software/437239/dicella-ecrf-clinical-trials> |
| en-NZ | <https://www.softwareadvice.co.nz/software/437239/dicella-ecrf-clinical-trials> |

-----

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