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Clinical trial software is the set of systems that collect trial data, randomise patients, and keep every form auditable.
Electronic data capture and trial platforms from Medidata (Dassault Systèmes; Rave), Veeva (Vault CDMS), Oracle (Clinical One), IQVIA (Orchestrated Clinical Trials), Castor, and Medrio run most oncology trials; eCOA/ePRO vendors (Clario, Signant, YPrime) capture patient-reported outcomes; RTSM handles randomisation and drug supply. Risk-based monitoring, direct EHR-to-EDC data flow, and AI-assisted data cleaning are reducing site burden.
Validated 21 CFR Part 11 systems with audit trails, edit checks, role-based access, and standards (CDISC CDASH/SDTM) for regulatory submission.
Query for this technology: (TITLE:"Clinical trial software" OR ABSTRACT:"Clinical trial software" OR TITLE:"EDC, eCOA, CTMS, RTSM" OR ABSTRACT:"EDC, eCOA, CTMS, RTSM") AND (cancer OR tumor OR tumour OR oncology OR carcinoma OR lymphoma OR leukemia OR leukaemia OR myeloma OR sarcoma OR melanoma OR glioma). Results are unfiltered search hits about Clinical trial software (EDC, eCOA, CTMS, RTSM), not a curated reading list.
Shares Clario, Contract research organisations (CROs) and the tag supporting.
Shares Oracle Health (Cerner) & Oracle Life Sciences and the tag supporting.
Shares Decentralised and hybrid clinical trials and the tag supporting.
Shares Decentralised and hybrid clinical trials and the tag supporting.
Shares Contract research organisations (CROs) and the tag supporting.
Shares Contract research organisations (CROs) and the tag supporting.
Shares Contract research organisations (CROs) and the tag supporting.
Shares Contract research organisations (CROs) and the tag supporting.
Open-source projects that implement or serve this technology, from OnCo's own catalogue: licence and last activity as the repository reported them on the day of the fetch. Listing is not endorsement; check the licence before reuse and the validation before clinical use.
Open electronic data capture for clinical trials, the community edition of a widely deployed EDC system.
A community fork keeping the open OpenClinica 3 code base alive and modernised.
The Dresden platform that connects trial data capture, imaging and radiotherapy plans for multicentre radiotherapy trials.
The Clinical Trials Transformation Initiative's relational database of the whole ClinicalTrials.gov registry, refreshed daily and free to query.
Shares de-identified comparator-arm data from phase 3 oncology trials with registered researchers at no cost.
A non-profit platform for sharing anonymised individual participant data from completed trials, including many oncology trials, on application and under a data use agreement.
Yale's Open Data Access project that reviews requests for participant-level trial data from partner companies.
Commercial and regulated products that serve this technology. Each card says what is behind it: a regulator's database, the literature, a public body's list, or only the company's own words. Listing is not endorsement, and a clearance is a regulatory fact, not a clinical one.
The public registry of clinical studies and the API almost every trial-matching product in oncology is built on top of.
Oncology real-world data and trial acceleration software, sold to sponsors and to the practices whose data it curates.
A de-identified oncology database assembled from the electronic records of the practices Flatiron sells software to, used for external control arms and regulatory submissions.
The data capture system most academic oncology studies actually run on, free to institutions in a consortium but not open source.
The search portal that federates the national trial registries, so a study registered outside the United States can still be found.
The European Union's single system for applying to run a trial and for publishing it, which replaced the old national applications and the EudraCT register.