Clinical trial management software, also known as clinical trial software or clinical trial management systems (CTMS), manages the operations, processes, and data involved in clinical studies and trials. A CTMS centralizes all trial and study data, standardizes and streamlines workflows, and tracks and optimizes site, participant, investigator, and trial processes. Pharmaceutical companies, medical research institutes, and research centers managed by hospitals utilize clinical trial management software. This type of software is used by CROs, medical researchers, and trial administrators or sponsors to plan, manage, and monitor the entire lifecycle of clinical trials. All CTMS are designed to adhere to industry regulation so that trials can maintain compliance according to both institution and industry.
To qualify for inclusion in the Clinical Trial Management (CTMS) category, a product must:
Compare Clinical Trial Management Software
Over 10,000 Clinical Trial Investigative Sites use the Florence Electronic Investigator Site File, Florence eBinders. The elimination of chaotic site-based processes enables electronic workflows that streamline the site experience and enable monitoring, startup, and source data verification remotely. Research operations with Florence are paper-free while maintaining strong global compliance. Advanced integrations reduce repetitive work by seamlessly sharing documents and data between site-based systems such as EMR, EHR, CTMS, eConsent, and IRB portals. Florence offers a complete site-based platform for electronic workflows with ease of use that makes the life of sites easier and facilitates over 3 million research actions every month.
Medidata CTMS was created with powerful modules for outsourcing, site monitoring and site payments you can turn on together or separately as you need them.
nQuery is now the world’s most trusted sample size and power analysis software. In 2018, 91% of organizations with FDA approved clinical trials used nQuery as their sample size calculator. It is used by Biostatisticians of all levels of expertise. Created by sample size experts, nQuery boasts an extensive list of easy-to-use but powerful features for sample size calculation and power analysis.
ResearchManager developed three eClinical tools: EDC, CTMS & ERMS Try the EDC & CTMS & ERMS configurator → https://form.jotform.com/RM21/G2 ●Electronic Data Capture | EDC: collect, validate and enrich clinical data ●Clinical Trial Management System | CTMS: effectively manage and track the entire study start-up & portfolio ●Ethical Review Management System | ERMS : Medical Ethical Committees can review & manage all clinical study protocols in just one environment. Book a demonstration: ➞ https://form.jotform.com/RM21/demo-request References: We have references in various sectors, such as: Medical Devices, Pharma & BioTech, CROs & Investors, Aademic institutions, Healthcare and Institutional Review Boards (IRB). Compliance: ReesarchManager conforms to 21 CRF PART 11, HIPAA, GCP & GDPR compliance. We are also ISO75001 & NEN7510 certified .
The OpenClinica Enterprise Edition is an enhanced, fully-supported build that is ideal for mission-critical settings.
Academic medical centers and cancer centers manage hundreds of protocols at once in an environment where there are many other, often competing, concerns ranging from limited resources to meeting ever-changing regulatory requirements. Furthermore, gaining visibility into operations and maintaining effective communication across research groups can pose significant challenges. The OnCore® Enterprise Research system, the leading enterprise-class clinical trial management system (CTMS), has a long history of successfully addressing the broad spectrum of challenges. Built in close collaboration with leading research institutions across the US, OnCore provides unmatched visibility into your research portfolio, delivers more compliant billing workflows, integrates with your enterprise systems, offers comprehensive reporting and analytics, and more.
Castor is a cloud-based Electronic Data Capture, eCRF, ePRO, eCOA, eConsent, and Decentralized Trials platform that enables researchers to easily capture and integrate data from any source in real-time. Highlights: ● Decentralize your trials with Castor eConsent, ePRO, and video. ● Build a study within hours using an intuitive form builder ● 90% of studies in Castor are built and pass UAT in less than 4 weeks ● Capture patient, clinician, EMR/EHR, and device data on a central platform ● Monitor study progress through real-time reporting ● Compliant with 21 CFR Part 11, GCP, GDPR and HIPAA ● ISO27001 and ISO9001 certified ● Top-rated EDC and ePRO systems ● World-class support