Alternatives to Chronicles CTMS
Compare Chronicles CTMS alternatives for your business or organization using the curated list below. SourceForge ranks the best alternatives to Chronicles CTMS in 2024. Compare features, ratings, user reviews, pricing, and more from Chronicles CTMS competitors and alternatives in order to make an informed decision for your business.
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OpenText for Life Sciences
OpenText
OpenText™ Information Management solutions help life sciences organizations leverage insights from data and content to improve decision-making processes and accelerate product development. Integrate, manage, and securely exchange data across people, systems and things. Leverage information assets from R&D to commercialization. Freedom of choice with cloud-native software that can run anywhere. OpenText for life sciences accelerates the discovery process by extracting actionable insights that drive pipeline innovation. Capture and manage research papers into electronic lab notebooks with intelligent capture. Find insights with text mining. Extract knowledge trapped in the unstructured text contained in clinical trial reports, study protocols, clinical safety and efficiency findings. Find out how to intelligently analyze, classify and extract clinical trial documents to reduce the risk of costly stops and starts. -
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IBM® Clinical Development provides pharmaceutical, contract research organizations and medical device companies unified technology from start up to submission to support clinical trials. With our clinical data management system, users can organize and analyze report data from anywhere in the world. Enabling pharmaceutical organizations to deliver therapies faster to their patients. Design and launch studies without database migration. Deliver quick and easy remote consent with minimal integration.
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GRAVITY
ASSAY Clinical Research
In clinical research, being organized is a prerequisite of success. Bringing the right resources to bear at the right time is a challenge. This is particularly applicable for document management for a clinical trial. GRAVITY is your long-time solution for site file and trial master file management. We have converted both files into easy to manage, co-ordinated electronic format. This integrated package facilitates logical and convenient document management. Being an integrated eTMF and eISF system, GRAVITY becomes a complete cloud-based electronic DMS, Serving as a window for sponsors, CROs, and Sites. However, GRAVITY can also be deployed and utilized for each individual entity alone. when a site is selected for conducting clinical trial, Documents start to flow in, however, the initial pack of essential documents require maintenance. GRAVITY incorporates a unique features of overseeing the essential document management and alerting the users of expiring documentation. -
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Datatrial Nucleus
Datatrial
One Platform to Research, Document, and Collate your Clinical Data. Simplify your research data with the Nucleus platform. A single platform to store your study documentation, clinical datasets, submission data and compliant media. Nucleus Documents enables document management and version control for your quality documentation and media. Control, manage, and share company content with ease. Collate and control your electronic trial master file documents with ease using our centralized regulatory document management solution. Nucleus Coding enables dictionary term coding against both MedDRA and WHODrug dictionaries, either in our standalone application, or integrated into your data capture system. -
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Clinical Research IO
Clinical Research IO
The industry’s leading eSource, CTMS, and eRegulatory software for clinical trial sites. Capture source data seamlessly and in real-time with CRIO’s best-in-class electronic source. You’ll eliminate up to 90% of your paper and improve data quality by 80%. Take control of your operations with CRIO’s intuitive Clinical Trial Management System. Schedule patients, track financials, streamline recruiting, and more. Introducing electronic regulatory binders fit for the 21st century, which includes the first-ever electronic delegation log — all 21 CFR Part 11 compliant. For clinical trial sponsors: conduct 100% remote monitoring of your sites’ source data and regulatory documents in a secure, online portal. Join Our Network of 500+ Clinical Research Sites From Around The World. Our mission is to help you grow your business. We do that by streamlining your site’s operations, so that your studies don’t stop just because you aren’t in clinic. -
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QureClinical
Quretec
As a Data Management provider we offer data management and statistical analysis planning and model development with applicable CRF design. All the appropriate documentation is provided by us according to FDA and other regulations. Previous experience has shown us that putting more effort into the planning phase will give a better, faster and efficient result in the end-phase of the trial. Our databases are generated by experienced data managers who have worked with several eCRF-s and already know the critical parts of the electronic data capture system design and data collection. This allows the eCRF to be built in a short period of time. eCRF validation and testing is compulsory part of the design and is dealt by different personnel in order to receive a hundred-percent elaborated eCRF. -
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Clinion eTMF
Clinion
Clinion's electronic trial master file (eTMF) system has unique features that simplify storage, access, and management. The simple user interface makes it the go-to tool for clinical trial document management. -
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Clinical Conductor CTMS
Advarra
Clinical Conductor CTMS is a cutting-edge clinical trial management system (CTMS) designed for hospitals, research sites, asset management companies, site networks, health systems, and contract research organizations (CROs). This cloud-based solution helps make the clinical trial process more efficient, thereby helping research organizations make better business decisions and meet every challenge. Key features include electronic data capture, study planning, enrollment management, document management, recruiting management, and more. -
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BizNet
Sarjen Systems
Consists of clinical trials management solution suites for various CROs, Pharmaceutical, Biotech and Medical device industries. BizNET-CTM, is a multi-functional platform which allows a CRO (Contract Research Organization) in planning, managing, designing, executing, monitoring and analyzing trial related activities and data in adherence to the protocol obligations and regulatory requirements. An end-to-end solution suite which cater to the needs of clinical research project starting from Project Management, feasibility assessment, volunteer or patient enrollment using iris recognition technology, capture clinical trial data, multi-level review process, data compilation to data archiving. The BizNET-CTM suite is designed to manage all of the documents, tasks, processes, relationships, audits, and training that must be administered and controlled throughout the life of a clinical trial. -
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Medidata
Dassault Systèmes
The Medidata Clinical Cloud is our cutting-edge platform that transforms the clinical trial experience for patients, sponsors, CROs, and research sites. As the only unified technology platform dedicated to clinical research, the Medidata clinical cloud addresses the holistic research process from start to finish. Our platform helps life science and medical device organizations cut development costs, mitigate risks, and deliver treatments and devices to market faster. No matter which products you choose for your clinical trial program, you will have access to the power of the Medidata Clinical Cloud. At Medidata, we’re leading the digital transformation of clinical research. Powered by artificial intelligence, machine learning and advanced analytics, our platform brings researchers, study managers, investigators, and patients together to accelerate research. Obtain regulatory-compliant, patient-friendly electronic informed consent for clinical trials. -
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AcceleTrial
LINEA System
AcceleTrial™ takes the guesswork out of clinical trial site identification and activation. Our Study Start-up Management System (SSMS) is based on the foundation of objective data and not self-identification. AcceleTrial™ gives you a database of thousands of sites globally that are ranked and indexed on the basis of: Objective Site-specific Therapeutic Expertise, Objective Site-specific Clinical Trial Experience and Objective Patient Data. Objectively pair the right sites globally with objective data on expertise, experience and patients to your clinical trials. Expediently launch the right sites to begin enrolling patients using AcceleTrial™ automated “push and pull” structure presented in multiple languages. Accurately collect required documents using pre-filled templates and track activities in real-time. Immediately start using system – cloud-based solution requiring minimal IT set-up or training. Simply integrate AcceleTrial™ with CTMS or other clinical trial systems. -
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Astracore Clinical Trials
Astracore
Our clinical trials management system is suitable for virtually any controlled clinical trial, including randomized trials, with a choice of randomization algorithms. Clinical trial software is easily configured for paper CRF (Clinical Report Form) and provides eCRFs (electronic CRF). The software can be configured to capture data in a vast number of forms and techniques, with specific rules as defined by you, to build in integrity and quality checking. The system can be used for direct Electronic Data Capture (EDC), i.e. eCRF, or to print paper CRFs which could consequently be entered into the system. You can also attach images, audio, video, documents (say consent forms) etc., limited only by the amount of storage available. The system is Double Data Entry enabled and has detailed exception reporting. This includes and option to lock records once they have been matched, to prevent any further changes. -
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Clienvo eTMF
Clinevo
Clinevo electronic Trial Master File (eTMF) is an easy-to-use electronic Trial Master File in electronic (digital content) format for organizing and storing documents, images, and other digital content of clinical trials. Clinevo electronic Trial Master File (eTMF) has an inbuilt DIA reference model and meets regulatory guidelines. Clinevo MICC Intake is a web-based tool for Medical Information Call Center (MICC) and PV users to Log, Track and Monitor Product Quality Complaints (PQCs), Medical inquiries (MIs) and Adverse Events (AEs). Clinevo Safety is a cloud-based, user-friendly, easy-to-use, regulatory-compliant end-to-end Pharmacovigilance / Drug safety system. The All-in-one system provides PV Intake, Case Processing, Regulatory Submissions / AS2 Gateway, Analytics, and Safety signals capabilities under one platform. Clinevo Website Intake is a web-based tool which can be connected to Sponsor / CRO websites to provide Consumers and Reporters a User friendly web interface. -
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LifeSphere eTMF
ArisGlobal
LifeSphere eTMF is your clinical trial’s single source of truth. Discover a versatile solution that streamlines inspections, ensures compliance, and saves your organization time and effort. Built as the first system to support the TMF reference model, LifeSphere eTMF aligns Clinical documentation with regulations and study protocols in one solution. Create and manage a single source of truth for your clinical trial. Ensure trial master file quality, timeliness, and completeness with live collaboration and real-time document sharing. Streamline TMF inspections quickly and efficiently to handle any audit. Maintain compliance with embedded workflows and dashboards that allow easy trial reconstruction. -
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ePharmaSolutions
ePharmaSolutions
At ePharmaSolutions, we are building something new. We are not a high-tech company. We are an idea company whose thinking is highly entrenched in technology, but not limited by it. We support the drug development industry with solutions that improve the identification, activation, training and management of clinical trial sites. With new perspectives on old problems, we deliver technology-enabled solutions that help to “un-complicate” the chaos of clinical trial management. ePharmaSolutions (ePS) is a leading provider of e-clinical solutions that improve the way that clinical trial sites are selected, trained, activated, and managed. By applying fresh thinking to old problems, we deliver clever, technology-enabled solutions that empower sponsors, contract research organizations and investigator sites to “un-complicate” the chaos of clinical trial management. -
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Healthcare solutions from VACAVA reduce the complexity and cost of clinical trial regulatory document management. Each time documents move through a manual workflow, it introduces the opportunity for delays and lost information. VACAVA solutions help you streamline regulatory processes by storing profiles, forms and documents in a single easy-to-access online location. Documents seamlessly move through your workflow with approvals captured electronically (21 CFR Part 11 compliant). Easy-to-read dashboards enable efficient management. VACAVA’s Regulatory Document Management System was built in collaboration with a major clinical trial research base to simplify operations and radically increase efficiency. VACAVA’s Regulatory Document Management System is surprisingly affordable and can be customized to meet your unique needs. VACAVA’s solutions are flexible, scalable, and delivered via the cloud so you never have to worry about managing servers, security, and backups.
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Data MATRIX
Data MATRIX
All-in-one diamond SaaS solution for clinical trials. Data MATRIX team has been working with clinical data since 2009. We process data, analyze it and develop documents to be accepted by the Russian Ministry of Health, FDA, and EMA. Our products automate the processes of clinical trials, and users manage and monitor its progress online. We adjust and validate our software before the project starts and take into account all aspects of the project in order to do it in the best way. Our team has conducted 180 projects for pharmaceutical and biotech companies and CROs. With Data MATRIX products, 6 out of 10 TOP Big Pharma companies reduced their R&D costs by 15%. Our employees are proud to be members of professional communities which unite clinical data specialists (CDISC), data managers (ACDM, SCDM), biostatisticians (ISBC), and medical writers (EMWA, AMWA). -
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Simple Trial
Trial by Fire
SimpleCTMS was designed and developed to offer the benefits of a CTMS (Clinical Trial Management System) without the extensive upfront financial and resource commitments associated with traditional enterprise systems or the inherent inefficiencies of worksheet trackers. SimpleCTMS provides early-stage drug developers a scalable and cost-effective solution to improve the management, performance and study startup costs associated with clinical trials. A dedicated client manager provides pro-active support and guidance. All users receive technical support from our team of clinical software experts. Customized training and professional services are available at additional cost. Backed by a quality system using validated software processes.Starting Price: $399 per month -
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Clindex
Fortress Medical Systems
A Clinical Data Management System (CDMS), Clinical Trial Management System (CTMS) and Electronic Data Capture System (EDC) all in one powerful, integrated solution. All your study information can be at your fingertips with our innovative, flexible and compliant Clinical Trial Software System. Our servers or yours. Clindex® can be installed on your servers or it is available on the Fortress Medical Cloud (SaaS – Software as a Service). Cloud access is available world-wide and your data is securely stored at a SOC 3 certified data center. You can build, we can build. Clindex® provides all the tools you need to develop your own study database. Our quick start manuals and help documentation walk you through the process, step by step. Or our Clindex services team can develop a study for you. -
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Veeva SiteVault
Veeva Systems
Streamline regulatory operations across your organization to improve compliance and advance research. Veeva SiteVault reduces the complexity of conducting clinical trials by connecting your regulatory operations to improve efficiency and compliance. Manage regulatory and source documents in a single system that supports 21 CFR Part 11 and HIPAA requirements. With a real-time visibility across trials, SiteVault Enterprise improves operational efficiency, speeds study activation, and enables faster, higher-quality trial execution. Replace manual processes and design your own workflows to support quality and speed study activation. Eliminate the need to grant EMR access or redact documents by providing monitors with secure, direct access to your regulatory and source documents. Create your own workflows, reports, and dashboards for greater visibility into start-up timelines and regulatory processes. -
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Phoenix CTMS
Medical University of Graz
Phoenix CTMS is a modern web application combining the capabilities of database software used in clinical research in one modular system. After years of collaborative development with trial sites at the Medical University of Graz, the Phoenix CTMS now becomes publicly available (LGPL 2.1). This unmatched feature set is geared to support all operational and regulatory requirements of the clinical front end in academic research, at CROs (Contract Research Organisations) and hospitals conducting clinical studies of any phase. want a CDMS that gives you unlimited Javascript form scripting support (server- and browserside). You need to deal with large eCRFs (electronic case report forms) want to try a serious open source alternative for eCRFs. Need to formulate complex ad-hoc database queries to list matching subject candidates using set operations. Conduct several trials in parallel and need to organize site staff and resources. Need a software to implement various processes for ICH GCP.Starting Price: $1 one-time payment -
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Ofni Clinical
Ofni Systems
Ofni Clinical is a clinical data management tool that rapidly creates and implements secure, regulatory compliant clinical trial databases. Ofni Clinical includes comprehensive search and report features, has strong data validation and edit check options, contains flexible customization tools, and can be implemented quickly and economically. The databases can be used to capture data from existing paper Case Report Forms or as paperless electronic data capture systems. Many Ofni Clinical projects require less than a month to go from project initiation to validated implementation. Contact us today and find out how to use Ofni Clinical for your clinical trials. Matches your existing Case Report Forms (CRFs), reducing training and implementation costs while adding electronic data capture and review capabilities. Includes extensive edit check and data validation features to identify questionable data entry and support data analysis. -
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MAISi
Agile Health Computing
Until now, the options available for managing clinical trials at an investigator site were either keeping multiple shared spreadsheets or buying expensive software unsuited to Australian conditions. MAISi is the game-changer. Beginning as a repository for clinical trials data at a major hospital in 2001, MAISi has evolved into a sophisticated workflow application to assist in most aspects of a research unit’s operations. MAISi acts as a central repository of data to store information about studies and the business units that run them. The datasets are arranged to support management decision-making. Staff in each business unit have access to the data (Studies, Patients, Investigators, Study Team Members) associated with their own business unit, whereas staff granted global access (normally Financial Officers and System Administrators) have access to all data. -
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Protocol Manager (CTMS)
Atlant Systems
Protocol Manager helps clinical operations manage global trials of drugs, devices, biologics, and vaccines in all phases of development. When the appropriate Standard Operating Procedures (SOPs) are implemented in your company, Protocol Manager can help you be compliant with the FDA’s 21 CFR part 11 regulations. Protocol Manager supports Web Services technology to provide seamless, automatic integration with many popular EDC and IVRS products. For systems not supporting Web Services, integration is supported via an export/import mechanism. A robust tracking tool and database designed to manage myriad trial information and metrics. -
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ClinAccess
MAJARO InfoSystems
ClinAccess™ 5.1 is the next generation of our industry leading Clinical Data Management System based entirely on SAS® 9. It leads the way in simplifying clinical data management, clinical trial analysis and preparation of electronic submissions. Having your data keyed directly into SAS® data sets enhances your staff’s productivity by eliminating the time spent transfering data from Oracle/SQL into SAS. ClinAccess™ is designed expressly for ease-of-use study definition, data entry and management with features to monitor the progress and quality of ongoing clinical trials. Whether for review, analysis, or FDA submission, your data is always in SAS®and ready for analysis. The database structure is designed to support and accelerate statistical analysis and reporting. The result is less time and effort for data analysis and a shorter time to market. For reliability, auditing and security, there is no better solution than ClinAccess™. -
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Trials.ai
Trials.AI
Our Smart Protocol system aims to automate and add intelligence to clinical trial design with AI. Our Smart Protocol solution is revolutionizing the manual way research teams design clinical trials. In the digital age, humans cannot physically read and digest every bit of information relevant to a given decision. In addition, almost every company has valuable data that is not being used - more often than not, documents are living in repositories with no line of sight. As a result, companies life science companies are making important and costly decisions with incomplete information. We aim to take companies like yours from a document-driven environment into a data-driven one. We are reimagining how clinical trials are researched and planned by removing the barriers between data and end-users. We do this by mining massive amounts of trial-related documents from both customers and the public domain— so you don’t have to.Starting Price: $20 per month -
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Over the last several years, the Life Sciences industry has faced nearly $15 billion in fines and compliance-related settlements, making it critical for companies to adhere to pharmaceutical, medical device and biotech best practices. Efficient and effective management of clinical trials can also significantly impact the time, scope and budget for the development of a drug or medical device. With OpenText™ Clinical Trial Quality Management System (ctQMS), companies can remain compliant, reduce costs of records management and establish best practice through collaboration before, during and after the clinical trial lifecycle.
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Trialpack Designer II
Fleximation
Trialpack Designer is an easy-to-use and powerful tool to design blister packs and cards for clinical trials. It is particularly well suited to design packages for complex blinded trials such as dosage titrations, double-dummy and cross-over trials where a pack contains a range of different products. It provides configuration data for the Trialpack PC Controller, the Trialpack Controlled Dosing Systems and the Trialpack Robotic Packaging Systems. Direct and easy on screen design of blister shapes, print images and filling patterns. Highly granular user access rights. Workflow features with electronic signatures. Detailed 21 CFR Part 11 compliant audit trail. Reports with detailed packaging instructions and material requirements. -
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Transition Technologies eCRF
Transition Technologies Science Sp. z o.o.
Flexible eCRF platform for non-commercial clinical trials, configurable to any clinical trial study protocol. Our eCRF solution was created on the basis of many years of experience of researchers and medical teams with whom we carried out research projects. The system is, above all, easy to use, user-friendly and extremely flexible. The prepared solution meets all the required quality standards, and thanks to the full control over the code, we can further develop and adapt it to the changing requirements of regulators and the clinical trials market.Starting Price: $45k licence -
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Replior
Replior
An integrated EDC, eConsent, ePRO and Virtual Visit platform for the efficient conduct of clinical trials. Replior is a company providing software for clinical trials. Our suite of systems is called Trial Online and enables collection and management of data from investigators, participants and wearables in an easy and efficient way. Trial Online supports decentralized clinical trials (DCT) by enabling the trials to operate with site visits, remote visits or as a hybrid. We started our journey 20 years ago with a request to build an online CRF service for one of the world’s largest pharma companies, back then we were an IT operations provider for the pharma industry. This was the starting point of providing software for collection of data in clinical trials. Today we offer a full suite of data collection software services, and our IT operation is performed by our, very certified, sister company Complior. -
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InfoEd Global
InfoEd Global eRA Research
Turnkey research management solutions are designed to help you obtain funding, deliver results, and manage everything in between, faster and better eRA Research Software. Worldwide, more leading research institutions, universities, and corporations have chosen the InfoEd Research Software Solution to realize cost savings, improve data integrity, manage administrative processes, and accelerate compliance for electronic research administration versus any other research compliance software or eRA software. Our core belief is that industry experience and knowledge are the foundation of superior software development in the research administration software field, which has resulted in an unparalleled suite of research support technological applications, professional services software and industry educational programs by InfoEd Global designed specifically transcend today’s modern research institution.Starting Price: $1 one-time payment -
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PRA Prism
Nextrials
Data comes at you from all directions – EDC, EHR, smartphones, mobile devices, central laboratories. Prism assimilates data from these disparate sources and transmutes them into information and ultimately knowledge. Prism EDC combines ease-of-use with innovative features to provide a fresh solution for the collection and management of clinical trial data. Prism offers more that than form-based data collection, it aggregates and manages data from a myriad of data sources. Prism eSource is an innovative software solution that allows research teams to extract clinical trial information directly from a site’s electronic health record (EHR). This creates efficiencies and cost savings beyond the current paradigm where sites must enter the same data in multiple systems and accelerates the delivery of novel therapies to patients. -
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Longboat
Advarra
Longboat is a cloud-based clinical trial support solution provides users with an integrated Guided Compliance toolset to guide them at all times. Longboat provides the clinical trial site staff with the right resources to let them focus on patients. Longboat allows patients to view essential study information and check visit reminders. Longboat allows users to seamlessly manage the controlled rollout of the amended clinical trial protocol. Centralize the secure exchange of regulated documents between sponsors, CROs, and sites, significantly streamlining study startup and eliminating historically cumbersome processes across research stakeholders. All key stakeholders—clinical operations, monitors, site staff, and participants—access one integrated support platform with content tailored to meet their specific needs. Provide your site staff the tools and resources they need to stay engaged and compliant while focusing on the participant. -
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Complion
Complion
Complion’s platform is the accepted standard built specifically for clinical researchers. Our solution ensures the highest level of compliance with the greatest efficiency and the least amount of work. Allowing you to focus on what really matters — advancing and improving patient outcomes. Whether you are a Research Site, Sponsor or CRO, our eReg solution can help you address any type of clinical trial challenge, now and in the future. Reduce costs, avoid redundancy, and increase staff productivity. Easily archive, get signatures and view files from anywhere or from any device. A built-in audit trail ensures accuracy and eliminates study conduct and patient safety risks. Our clients include leading cancer centers, medical centers, hospitals, and health systems, as well as multi-specialty practices and dedicated research sites. -
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Clinibase
Cardiobase
Our platform offers the comprehensive support that your clinical trial needs using cutting-edge cloud-hosted technology. Clinibase will help your organization realize significant gains in efficiency and productivity. We do not adopt a plug-and-play approach with our Clinical Trial Management System. Why? Because we believe that every organization has unique systems and processes. Therefore, Clinibase can be fully customized to fulfill your organization’s clinical trial needs and requirements. Furthermore, we use surveys to troubleshoot, recognize areas for improvement, and automate all components of your daily clinical trial processes. Quickly locate eligible participants with our social integration tools to recruit them faster. Keep your participants engaged with smooth communication tracks that enable high retention and foster positive participant experiences. Enhance the validity of your trials knowing that data is recorded accurately and stored safely. -
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RealTime-CTMS
RealTime-CTMS
RealTime-CTMS is a premier, cloud-based clinical trial management system (CTMS) purpose-built to boost efficiency and profitability for site networks and research sites. Comes with fully-integrated services that include RealTime-PAY, RealTime-TEXT, and RealTime-eDOCS (the first fully-integrated eRegulatory document management system), the solution promotes quicker and easier access to subject or study information using simple and intuitive navigation. RealTime-CTMS offers a host of other solutions that covers online document storage, appointment reminders, data collection, payment processing, among others.Starting Price: $295.00/month -
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CTMS Master
Anju Software
Premier clinical trial management system designed specifically to help overcome technical challenges associated with managing clinical trials. CTMS Master improves user accessibility and communication, reduces manual operations, and eliminates redundant data and tasks, allowing a more efficient trial conduct. An integrated Site Visit Report tool with automated workflow eliminates duplicate data entry and facilitates the creation of out-of-the-box Site Visit Reports (SVR). Maintain standard templates for project and site documents, events, milestones, site visit reports and budgets that are tailored as needed for each study. CTMS Master provides 100+ metrics/statistics for clinical study projects, countries and sites as well as 80+ standard reports plus ad hoc reporting capabilities. With CTMS Master, you can define site-specific budgets from a default budget template, track accrued payments and future obligations, define automatic or manual approval of each payment type, and more. -
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ClinSoft
Innovate Research
Innovate’s End-To-End Clinical Data Management Services. Our clinical data management processes, expertise and technology are developed to make each step of your clinical trial data management process more accurate and efficient for Phase I-IV in wide range of therapeutic areas. Our CDM Team Is Well-Versed With Current Good Clinical Data Management Practices (cGCDMP) International conference on harmonization Good Clinical Practices (ICH-GCP) 21 CFR Part 11 Compliance Health Insurance Portability and Accountability Act (HIPPA) Requirements Applicable Regulatory Guidelines SAS datasets SAS XPORT transport files EDC Helpdesk Support 24/7 On-Site and Off-Site Clinical Data Management Services Electronic Data integration and transfer Quality Control Activities Medical Dictionary for Regulatory Activities (MedDRA) Serious Adverse Event (SAE) Reconciliation Clinical Database Transfers Clinical Database Lock paper Case Report Form (pCRF) and electronic Case Report Form. -
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QMENTA
QMENTA
Globally accessible, infinitely scalable, AI-powered, collaborative cloud platform meeting the highest standards of security and compliance. An industry-leading and simple-to-use software platform, purpose-built by neuroimaging and data science experts to meet the distinct and challenging needs of the neuroscience community. Optimized and tailored for your needs, whether you are conducting research, running clinical trials, at the point of care, developing novel algorithms or leveraging brain-related data. Global data aggregation, and consolidation of imaging-based studies in one cloud platform. Streamlined, end-to-end clinical, real-world data and medical imaging data management. End-to-end expert and personalized support to ensure your study success. Centralized reading and the ability to compare quantitative results to a normative database. Highest quality, shareable reporting and data exporting for submissions approval. -
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Cronos
Webosphere
In-system protocol & its a training program. Equipped with fingerprint attendance. Cronos provides highly customizable if/workflows capable for conducting derma/ patch/ other BA-BE/ early phase studies. Capture, cleanse and efficiently manage your study data from paper-based or EDC-based trials. Extract data in desired datasets following standards like CDISC (SDTM). EDC tool with real-time activities. It’s Bedside Data Collection capabilities help in paperless & faster assessments. It comes with a sample inventory & tracking facility as well. Compliance-ready data repository.The facility of data e-printing from almost all BA instruments/software and online review of data in defined workflow with e-stamping and e-signature.Project-wise view, export & archival of data. Generate high-quality statistical reports (tables, listings & formats) in fixed/desired formats with ease. -
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Leapcure
Leapcure
Leapcure is a leading patient recruitment and engagement platform that connects clinical trial sponsors with eligible patients. Utilizing advanced technology and strategies, we enhance trial participation and improve patient outcomes. Our platform streamlines the recruitment process, ensuring that trials are populated with suitable candidates quickly and efficiently. Leapcure is dedicated to advancing medical research by making clinical trials more accessible and effective. We work closely with sponsors and patients to facilitate smooth and successful trial experiences, ultimately contributing to the development of new treatments and therapies. -
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Dacima Clinical Suite
Dacima Software Inc.
Dacima Clinical Suite is the most advanced web-based solution that combines electronic data capture (EDC), clinical data management software (CDMS), and clinical trial management software in a single platform. Built for clinical trials, epidemiological research, web randomization (IWRS), ePRO, web surveys, and patient registries, Dacima Clinical Suite helps efficiently streamline the clinical data collection process. Dacima Clinical Suite consists of three core modules: Manager (Administrator) Module, Designer Module, and Data Entry Module. -
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Cloudbyz CTMS
Cloudbyz
Cloudbyz CTMS is a cloud-based trial management platform natively built on Salesforce Cloud. It is aimed at sponsors, clinical research organizations (CRO), and clinical sites for managing end-to-end clinical trial operations. Designed for clinical research, it expedites implementation and drives user adoption. Cloudbyz CTMS comes with an intuitive, straightforward design that allows for quick deployment. Boasting a rich set of features, Cloudbyz CTMS makes it easy for users to manage all aspects of clinical trials, including sites, enrolment, documents, events, milestones, site visit reports, finances, inventory, etc. Cloudbyz provides end-to-end management of the clinical trial lifecycle, including study setup, site management, study projections, monitoring, and financial management. With Cloudbyz, you can optimize your study planning, accelerate patient recruitment, and increase trial quality, while reducing costs and minimizing risk. -
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TrialPoint
Databean
TrialPoint™ electronic data capture (EDC) is easy to configure, easy to use, and the coordinators love it. Our data managers are experts in converting clinical protocols into geek-speak (metadata dictionaries for those in the know) and will configure TrialPoint™ to work for you, not against you. The system can accept any randomization string, media upload, or coding dictionary. It can even blind users to treatment assignments. To promote time-sensitive data collection. the system will prospectively calculate visit windows and send out alerts and reminders keeping the team focused and on task. Nowadays, patient-reported health outcomes and quality of life questionnaires are included in most trial designs and are responsible for many protocol compliance issues. Take a look at TrialPoint’s electronic patient-reported outcomes (ePRO) module which can be configured to fit any quality of life questionnaire or patient diary. -
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Mednet
Mednet
Mednet is a healthcare technology company specializing in eClinical solutions designed for the global life sciences community. Mednet’s flexible, electronic data capture (EDC)-centric eClinical platform improves the efficiency of clinical studies of all types and sizes. Beyond simply EDC, Mednet’s comprehensive solution set provides the tools required to build and manage all types of clinical research, while adapting to evolving demands and requirements. Pharmaceutical, medical device, biotechnology and Contract Research Organizations (CROs) around the world have trusted Mednet for nearly 20 years to deliver the technology innovation, experience and reliability they need for success. For more information, visit mednetsolutions.com. -
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TrialKit
Crucial Data Solutions
Founded in 2010, Crucial Data Solutions (CDS) provides the most innovative low-code/no-code data and clinical trial management technology on the market today. TrialKit, our cloud-based platform available via both a web and native mobile app, enables end-to-end clinical trial management for medical device, diagnostics, digital therapeutics, and biopharm companies of all sizes. Design and deploy validated studies in days not weeks using our intuitive study builder that requires no programming. Thousands of global users have leveraged the flexibility of TrialKit to deploy over 8,000 studies across all phases of development, including Verily (a subsidiary of Alphabet), ICON, Catalyst Clinical Research, SISCAPA Assay Technologies, CDx Diagnostics, and Optinose, and many more.Starting Price: Upon request -
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Calyx
Calyx
At Calyx, we know that the success of your clinical development program comes down to data. Which makes the effectiveness of your electronic data collection (EDC) system key. Used in over 2,600 worldwide clinical trials, Calyx EDC streamlines clinical trial data collection and reporting—in one easy-to-use platform. Don’t trust your important data to just anyone. Contact us to learn how Calyx can propel your program’s success. Calyx EDC gives you the flexibility to easily plan, design, and conduct studies, regardless of their complexity. With features that help reduce costs, improve site visibility, and drive efficiency, Calyx EDC keeps your trial on track. -
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Catchtrial
Meditrial Europe
Catchtrial is the online electronic solution to manage CRFs and images with efficacy and speed. Simple, secure, affordable, Catchtrial has been chosen by leading manufacturers and small companies alike to manage their international trials. By replacing the paper-based process, Catchtrial ensures cost savings. No monitor visits to sites will be needed to collect paper CRF. You can also capture and upload images, so there will be no need to ship CD roms. Sponsors have full control of the study progress, simply by accessing the study from their offices. Compared to other eCRF offerings, Catchtrial offers special functionalities and flexible personalizations for unprecedented ease of trial management. -
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Teckro
Teckro
Teckro clinical trial software connects all study stakeholders to critical information. Every time. Everywhere. We find answers every day from our smartphones. Why shouldn’t the same be true for clinical trials? Critical, up-to-date study information always at hand when and where research staff and CRAs need it. Study answers are just a tap away on any mobile device, giving research staff a direct line to crucial details. And when updates or amendments are needed, site staff and monitors can be alerted in real-time. Cloud-based clinical trial software, Teckro is up and running quickly with nothing to install. It’s simple, easy and intuitive. Teckro is securely hosted and compliant with major industry regulations, including FDA 21 CFR Part 11. Only the right, approved version of study documents, means no more worrying about version management. -
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Randomize.net
Interrand
Unlimited trial duration, number of subjects, clinical sites, treatment arms and stratification variables, all for a one-time fee. Full support for double-blinded trials, including kit management, kit replacement and emergency unblinding. Randomize.net supports permuted blocked stratification, minimization and simple randomization algorithms. Configure randomization applications with the exact options and features you want. With Randomize.net's Web Service API, you can integrate randomization into your application. Full support for subject randomization and reporting available. Highly secure internet-based randomization service for clinical trials.Starting Price: $2,500 one-time payment