Top 21 Electronic Data Capture (EDC) Software SaaS Companies in May 2026

Raleigh, North Carolina, United States

Discover CISYS LifeSciences' latest solutions designed for your clinical research teams. Our innovative suite of tools, including WebEAS, WebCode, WebFXP, and WebFormX, and WebFXP, ensures seamless operations for clinical research organizations. Established in 1990, CISYS LifeSciences is a global leader in providing eClinical Solutions and Services for the Clinical Research Community. Our technology and services are geared towards reducing costs and timelines associated with clinical trials. Through collaborative partnerships with research organizations of all sizes, we enhance solution efficiencies while minimizing costs. At CISYS, we believe in fostering true partnerships where organizations collaborate to achieve common goals. Our suite of eClinical Solutions supports all phases of clinical trials and is available globally in both SaaS and hosted models. Our Sequence Platform offers modules that can seamlessly integrate or operate as standalone applications. Our Sequence Platform includes: Clinical Event/Endpoint Adjudication (WebEAS) MedDRA and WHO Drug Coding (WebCode) Site Portal/Secure Document Exchange (WebFXP) Patient Eligibility/Enrollment (WebPatient) Smart Forms (WebFormX) In collaboration with our strategic partner, 3D Communications, we are proud supporters of Get Stuff Done 4 Kids (gsd4kids.org), a nonprofit organization dedicated to making a positive impact on the lives of children facing challenges. At GSD4KIDS, our mission is to provide hope, joy, resources, and assistance to these children and their families, demonstrating that they are not alone in their struggles.

Reno, Nevada, United States

Founded in 2010, Crucial Data Solutions (CDS) provides the most innovative and affordable data collection and clinical trial management technology on the market today. TrialKit, our cloud-based platform available via a web interface and downloadable native mobile app, enables end-to-end clinical trial management for pharmaceutical, biotechnology, and medical device companies of all sizes. Design and deploy regulatory compliant studies in days instead of weeks using our intuitive forms designer that requires no programming. Thousands of global users have leveraged the flexibility of TrialKit to deploy over 7,000 studies across all phases of development.

Redlands, California, United States

iRIS, by iMedRIS Data Corporation, is world-class software for pre-clinical and clinical trials, integrating trial functions into an easy to use Web-based application. iRIS modules configure to the specific needs of institutions, creating client-focused programs that eliminate redundancy of data input while maximizing the productivity of trials and reporting. Essentially, iRIS is a suite of tools that assists with the management of time-consuming regulatory requirements. Significantly with iRIS, researchers find that their focus is not on managing essential reporting issues, formerly performed all in hard copy, but on their studies and subjects. Clients receive the most control of any system available, along with both Web-based and onsite training. For over a decade, iMedRIS, based in Southern California, has provided research facilities and institutions with a variety of iRIS modules. Backed by a dedicated team of developers, project managers, and customer support representatives, iMedRIS remains the conscientious forerunner of medical research software design and implementation. All current trends point to completely paperless clinical trial reporting with more research institutions realizing the need for electronic recording methods. The mission at iMedRIS is to provide each client with an integrated management tool with several options to better support each institution’s configuration requirements and needs. With the knowledge and support of the development team and management staff, iMedRIS strives to ensure each client is given the appropriate instruments for a seamless transition to a completely paperless research environment.

Montreal, Quebec, Canada

Dacima offers an electronic data capture (EDC) and clinical data management software for clinical trials and other research studies with surveys, ePRO, AEFI, patient registry, patient diaries, EMR, and more! Variety of services for database development, data management to web randomization. Customer-focused professional services and support to ensure your studies are deployed quickly and managed effectively. Our staff have extensive industry experience and training materials to ensure your studies run smoothly. To learn more visit our web page at http://www.dacimasoftware.com/

Berlin, Berlin, Germany

Clincase is an end-to-end EDC and clinical data management system providing a complete and integrated environment for the implementation, testing, and conduct of clinical trials for CROs, biopharmaceutical, and medical device corporations. It provides a comprehensive range of features and functionalities while seamlessly integrating ePRO questionnaires to streamline the collection and management of clinical trial data. Clincase keeps data managers, monitors, and sponsors connected to study performance and progress while encouraging increased study participants and site involvement. Clincase has almost 20 years of experience with EDC software. Our team has high expertise in Data-Management, Software Development, Clinical Research, Project Management, and Data Privacy. Meet Clincase, Your All-In-One Clinical Software Suite