--- description: Review of ShareCRF 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: ShareCRF | Reviews, Pricing & Demos - SoftwareAdvice AU --- Breadcrumb: [Home](/) > [Electronic Data Capture Software](/directory/4632/electronic-data-capture/software) > [ShareCRF](/software/357170/sharecrf) # ShareCRF Canonical: https://www.softwareadvice.com.au/software/357170/sharecrf Page: 1 / 3\ Next: [Next page](https://www.softwareadvice.com.au/software/357170/sharecrf?page=2) > Managing clinical trial data shouldn’t be a constant challenge. ShareCRF is designed to make your life easier, empowering you to set up and manage your study without the usual frustrations. Efficency Without the Hassle Why wait days or weeks to launch a study? With ShareCRF, you can configure your entire trial in hours. No coding skills? No problem. Our intuitive, user-friendly interface allows you to set up forms, workflows, and settings independently, without needing outside help or technical expertise. Compliance You Can Trust Regulations are non-negotiable, and ShareCRF was built with this in mind. Our validated software ensures your data remains secure, traceable, and ready for any audit or regulatory review. With ShareCRF, you don’t have to worry about compliance—it’s embedded in the platform. Adaptability That Works for You No two studies are the same, so why settle for a rigid system? ShareCRF adapts to your unique needs, whether it’s a straightforward study or a complex trial. Configure it to match your workflows and requirements, without compromising on quality or functionality. The Simplicity You Deserve We believe that managing your clinical data shouldn’t take away from your research. That’s why we’ve designed a platform that reduces complexity and gives you more time to focus on what really matters—delivering results. Join the researchers, sponsors, and CROs who have already streamlined their studies with ShareCRF. Because efficient, compliant, and adaptable data management isn’t just a nice-to-have—it’s a must-have. > > Verdict: Rated **4.8/5** by 44 users. Top-rated for **Likelihood to recommend**. ----- ## Quick Stats & Ratings | Metric | Rating | Detail | | **Overall** | **4.8/5** | 44 Reviews | | Ease of Use | 4.8/5 | Based on overall reviews | | Customer Support | 4.8/5 | Based on overall reviews | | Value for Money | 4.6/5 | Based on overall reviews | | Features | 4.6/5 | Based on overall reviews | | Recommendation percentage | 90% | (9/10 Likelihood to recommend) | ## About the vendor - **Company**: INETSYS ## Commercial Context - **Pricing model**: Other (Free version available) (Free Trial) - **Pricing Details**: Prices are based on the number of patients or records to be included in the study, the duration of the study and the different functionalities required in it (ePRO, Randomization, Medical Coding, Files, DICOM, Identifiable Data Encryption, Personalized Reports). There are special discounts for non-profit clinical research projects. - **Target Audience**: Self Employed, 2–10, 11–50, 51–200, 201–500, 501–1,000, 1,001–5,000, 5,001–10,000, 10,000+ - **Deployment & Platforms**: Cloud, SaaS, Web-based - **Supported Languages**: English, German, Portuguese, Spanish - **Available Countries**: Afghanistan, Albania, Algeria, American Samoa, Andorra, Angola, Anguilla, Antigua and Barbuda, Argentina, Armenia, Aruba, Australia, Austria, Azerbaijan, Bahamas, Bahrain, Bangladesh, Barbados, Belarus, Belgium and 208 more ## Features - 21 CFR Part 11 Compliance - API - Access Controls/Permissions - Activity Tracking - Alerts/Notifications - Approval Process Control - Audit Management - Audit Trail - CRF Tracking - Clinical Study Management - Configurable Workflow - Customisable Branding - Customisable Forms - Customizable Fields - Customizable Templates - Data Capture and Transfer - Data Extraction - Data Import/Export - Data Storage Management - Data Synchronization ## Integrations (4 total) - IBM SPSS Statistics - Microsoft Excel - SAS Viya - SAS Viya for Learners ## Support Options - Email/Help Desk - Knowledge Base - Phone Support ## Category - [Electronic Data Capture Software](https://www.softwareadvice.com.au/directory/4632/electronic-data-capture/software) ## Related Categories - [Electronic Data Capture Software](https://www.softwareadvice.com.au/directory/4632/electronic-data-capture/software) - [Clinical Trial Management Software](https://www.softwareadvice.com.au/directory/4623/clinical-trial-management/software) ## Alternatives 1. [Florence eBinders](https://www.softwareadvice.com.au/software/371223/ebinders) — 4.5/5 (83 reviews) 2. [Castor EDC](https://www.softwareadvice.com.au/software/109506/castor-edc) — 4.7/5 (204 reviews) 3. [Researchmanager – Clinical Research Suite](https://www.softwareadvice.com.au/software/108609/research-manager) — 4.2/5 (112 reviews) 4. [Flex Databases platform](https://www.softwareadvice.com.au/software/456034/Flex-Databases-platform) — 4.5/5 (13 reviews) 5. [Jeeva eClinical Cloud](https://www.softwareadvice.com.au/software/267792/jeeva-eclinical-cloud) — 4.8/5 (12 reviews) ## Reviews ### "Top platform and team\!" — 5.0/5 > **Marta** | *20 September 2024* | Pharmaceuticals | Recommendation rating: 9.0/10 > > **Pros**: The attention and support of your team for any problem or unforeseen event. > > **Cons**: It is difficult for me to point this out but it may be the lack of customisation when downloading PDFs. > > Very good platform for CRD development, very intuitive and easy to use by research teams. From the team, very good service, always ready to help and solve problems. ----- ### "SahreCRF: A Reliable and User-Friendly EDC Solution for Clinical Trials" — 5.0/5 > **Michal** | *11 August 2024* | Medical Devices | Recommendation rating: 10.0/10 > > **Pros**: A Reliable and User-Friendly EDC Solution for Clinical Trials. The platform allows for extensive customization of eCRFs to match the specific requirements of various study protocols, making it adaptable to different therapeutic areas. Lastly, the support team is prompt and knowledgeable, offering timely assistance and proactive engagement, which ensures smooth operations throughout the trial. Also, it provides a budget-friendly EDC solution without compromising on essential features, making it ideal for small to mid-sized companies or studies with limited resources. > > **Cons**: Reporting features may be less robust compared to other premium EDC systems, potentially limiting the depth of data insights available directly within the platform. > > Overall, ShareCRF is a strong EDC solution for clinical trials, particularly for organizations seeking a balance between functionality, ease of use, and cost-effectiveness. Its user-friendly design, customizable features, and reliable support make it a valuable tool in the management of clinical data. ----- ### "Easy and quick solutions for investigator initiated projects" — 4.0/5 > **José María** | *3 June 2022* | Hospital & Health Care | Recommendation rating: 8.0/10 > > **Pros**: Ease to use and how intuitive it. Also the help during the design phase. > > **Cons**: The lack of quality certificates. Last time that this was requested, they only had auditories reports. ----- ### "ShareCRF's opinion" — 4.0/5 > **LAURA** | *14 October 2024* | Pharmaceuticals | Recommendation rating: 9.0/10 > > **Pros**: I like most that it is really easy to use. > > **Cons**: The downloading of data because it is not as visual as others I have used > > My oversall experience is good, it ir really complete and intuitive for the investigators. ----- ### "Clinical study with Share CRF" — 5.0/5 > **Eva** | *25 September 2024* | Biotechnology | Recommendation rating: 10.0/10 > > **Pros**: Smooth communication, easy management, continuous assistance during all processes. > > **Cons**: None. Everything was fine working with Share CRF > > The services provided by Share CRF have been totally satisfactory, with continuous attention to the needs raised during the development of the study and after its completion. ----- Page: 1 / 3\ Next: [Next page](https://www.softwareadvice.com.au/software/357170/sharecrf?page=2) ## Links - [View on SoftwareAdvice](https://www.softwareadvice.com.au/software/357170/sharecrf) ## This page is available in the following languages | Locale | URL | | de | | | en | | | en-AU | | | en-GB | | | en-IE | | | en-NZ | | | fr | | ----- ## Structured Data