Clinsoft is a clinical research organization that helps users to perform industry-level research by staying compliant with industry standards. The platform enables users to perform different kinds of researches to maintain the safety and effectiveness of medications, devices, and other treatment regimens. Moreover, the clinical data management system is involved in all aspects of clinical trials from protocol development to reporting.
The solution allows users to access the project-specific database to get an on-screen generation of various reports for customer’s requirements. It offers various technologies to users to help in completing their research, such as CRF design, Medical coding, and Protocol Violations.
Clinsoft helps the team in their research through its services, such as in trial initiation, conduct, or custom training. It provides quality tools and services to the users according to their requirements throughout their research. Lastly, it offers complete support and integrity to customers throughout their clinical research.
eReconciliation is a software that allows users to compare records of data from any clinical and safety database and informs users if there is any change. The platform offers operational functions that help users in managing the whole reconciliation operations and keeps an audit trail of the whole operation. It helps drug safety managers to save their time, reduce errors, and offers compliance with industry standards.
The platform allows users to easily import and export records from any clinical databases such as CRF, etc. It automatically orders data in sequence to enable users to link never to miss any information.
eReconciliation enables users to manage, coordinate, and delegate all reconciliation operations and helps users in tracking all the updates during the trials. Users can export the reports and output files for data management and archiving. Lastly, it offers a complete service book to enable users to understand how it works.
Protocol Manager (CTMS) is a clinical trial management system that helps users to manage clinical operations and trials of drugs and vaccines in all the phases. The platform allows users to stay compliant with the FDA’s 21 CFR part 11 regulations when the SOPs are implemented. It enables users to manage all the subject visits, their check-in, and check-out timing.
The platform enables users to monitor the visits of their patients and helps in managing the documents of their patients. It allows users to manage the payments of their patients and keep track of it to ensure profitability.
Protocol Manager (CTMS) offers automation of processes to keep things running smoothly and comes with time and expense tracking and reporting. It manages all the contracts of the patients, and keep everything secure; it comes with industry-standard security. Lastly, it comes with an alert system which sends email in case of any issue.
ETQ Reliance is a platform that enables users to maintain the quality of their portfolios and data and allows users to comply with standards and optimize their core quality processes. The solution helps users in adapting to quality processes in response to business change and enhances practices to create competitive differentiation.
The platform also enables users to optimize those critical processes that drive excellence through quality, such as document control, employee training, and change management. Moreover, it allows users to build a culture of quality, which starts from step one of the product and service design processes and enables users to track quality processes across the organization.
ETQ Reliance empowers companies to keep pace with the increasing regulations and provides compliance solutions. Moreover, it enables users to incorporate certain risk-based thinking into operational monitoring. Lastly, it offers analytics and insights to users about their quality management to make better decisions.
Clinical Assay Management is a platform that enables medical organizations to create and manage assay plans to track the assay inventory of medical facilities. The platform allows users to minimize their exposure to risks and to be more certain in their clinical studies. It helps medical researchers to improve their teams’ productivity in their scientific endeavors.
The solution enables users to stay consistent with the gathering of information and management of clinical research data. Moreover, it allows users to streamline their processes and control their research study from the beginning to the end. The solution comes with advanced document tools that enable users to stay compliant with industry standards.
Clinical Assay Management records everything automatically, such as storage of documents, sample shipment receipt, etc. Moreover, it automates all the processes to accelerate the processes and helps in tracking the sample data. Lastly, it offers reports and analytics of documentation and processes to users.
DFdiscover is a comprehensive CDMS solution that enables users to meet the responsive needs of clinical trials. The platform helps users to query data values, resolve their queries, and provide reasons to support data values. It enables users to track their schedules, complex trial designs, and it automatically tracks missing CRFs.
The platform offers users both kinds of data collection sources such as electronic and paper sources and allows them to fit the data according to their needs. It enables users to validates and cleans their data and offers compliance tracking of the data to meet the standards of the industry.
DFdiscover allows users to have complete control over the software, and over its functioning, and regulatory standards. Moreover, it enables users to collect and add data, both offline and online, and users can manage their data easily. Lastly, its mobile app allows patients to report their symptoms in their database.
BSI CTMS is a solution that offers intelligent visualization of data for the clinical trials. The solution is packed with features that support the pharma industry, diagnostics sponsors, and CRO in their clinical trials. It delivers comprehensive functionality to researchers from the startup of their projects to its reporting section at the end.
The solution is easy-to-use and helps users in daily work, and it supports customers during their configuration as it requires no external system integrators. Moreover, it also comes with the lowest total cost of ownership and allows users to accelerate data entry processes.
BSI CTMS also comes in both cloud and on-premise form, and users can choose according to their needs. Moreover, it is compliant with industry standards GDPR and offers data protection to users. Lastly, it also enables users to plan and manage all of their projects and can keep track of all of their activities.
Clinion CTMS is a Clinical Trial Management System that transforms a clinical trial into a cohesive work environment. The platform brings unique insights across the product lifecycle and helps in uncovering the key details of the case. It offers feature-rich tools such as worksheets, documents, and other payment features in a single platform.
The solution offers compliance with the standards of the industry and allows users to keep everything secure. Moreover, it allows users to manage and study research in real-time at the same moment to save the researcher’s time. It allows managers to manage all of the study material and keep reports on everything.
Clinion CTMS sends alerts to managers and IP managers to know about the expiry of products and enables project managers to keep track of their inventory. Lastly, it allows finance managers to keep track of their expenses, and they can display milestone achievements through the dashboard.
MasterControl Clinical Suite is a platform that enables users to connect all of the clinical data, documents, tasks, and processes in a single place. The platform helps users in managing their clinical research and helps in unifying the volumes of information effectively. It allows users to streamline their operations and clinical tasks and offers a solution to reuse the information.
The platform is used worldwide as it helps life sciences companies to gather data and link it to accelerate their processes. It comes with the TMF reference model that allows users to plan and approve TMF artifacts more efficiently from the initiation of the study to its closeout.
It enables users to consolidate and streamline all aspects of GCP compliance and supports audits of all clinical programs. Moreover, it allows users to manage and connect information from different sites on a single dashboard. Lastly, it keeps users reminding about their deadlines and tasks.
TrackWise is an on-premise quality management system that brings all the quality processes in a single place and allows users to automate and manage them efficiently. The platform enables users to end the hassle of managing paper, fax, and email separately, and users can handle all of these processes through a single platform.
The solution allows companies to identify trends and prevent problems before they occur and enables users to have a comprehensive look at quality throughout the organization. It helps in ensuring regulatory compliance and allows users to create and submit their compliance reports manually. Users can integrate the solution with their other software, such as ERP or CRM, to ensure real-time interoperability.
TrackWise enables employees to send reports on quality events from anywhere or any software through its cloud-based intake capability. Lastly, it allows companies to extend their quality processes to third-part and external users to ensure compliance beyond their organization.
Qualio is a cloud-based quality management system that enables users to unite their teams, processes, and data to get their products in the market. The platform allows users to get the hassle out of their quality management, regulatory compliance, and corrective actions.
Moreover, the birth of the system is the result of data take from qualified experts and customers who were tired of burdensome paperwork. The solution grows as companies’ data grow and is flexible at all stages, such as from discovery to preclinical development. It offers feedback to users, which they need across a distributed workforce to get their data to the market timely.
Qualio enables users to get their scale anytime to get their product to the market. Users can track the change in the data and its distribution from the beginning to the end. Lastly, it allows users to control access to the documents and provides reports to users on operations.
cubeCTMS is a platform that enables users to monitor the clinical trials of patients and manage the information on the progress of each trial. The platform allows users to track all the issues and offers effective resource allocation. It informs users about the factors that can enhance the quality of their clinical trials.
The solution enables users to view and monitor the progress of clinical trials from anywhere while maintaining a level of risk prevention. Moreover, it helps users to improve their target enrollment through the distribution of resources. Furthermore, the platform also comes with an integrated PM solution that allows users to keep an eye on their tasks.
cubeCTMS also allows users to implement risk-based monitoring through various metrics and offers dashboards and calendars to manage their schedules. Lastly, its central monitoring feature makes it for the users to carry out overall management related to everything.
SimpleTrials is a Clinical Trial Management System that enables users to manage their patients’ data and do research work easily. The platform offers validation of 21 CFR Part 11 Compliant CTMS at an affordable price and offers feature-rich packages. Moreover, the platform has everything, such as documents, calendars, contacts, schedules, etc. to help researchers work effectively.
The platform also allows users to add custom fields that help in expanding the research work and allows users to track study, site, teams, and portfolios. Moreover, it comes with subject tracking and offers integration with subject screening and enrollment records.
SimpleTrials also comes with the support for DIA reference models or build the eTMF model and helps in managing tracking details such as version and build columns. Moreover, it includes reports and KPI performance metrics for a monitoring plan. Lastly, it also enables users to share custom reports across different functional areas of the CTMS.
Ennov CTMS is a solution that the life sciences department uses to conduct clinical studies, and it offers clear visibility into investigational sites. The platform helps in improving efficiency and reducing the costs associated with running clinical trials. It enables researchers to meet challenges such as automating scheduling, managing finances, and providing accurate reporting.
The platform allows clinical researchers to make better decisions and to ensure compliance and enables them to monitor patient recruitment and manage their finances. Moreover, it offers comprehensive directories to users to manage site personnel and other people of the organization.
Ennov CTMS allows users to track patient visits, their histories, activities, drug supply, and allows them to receive and answer queries. Moreover, users can have complete visibility to the status of each study directly from the dashboard and can generate reports in each study. Lastly, this web-based solution allows users to access it from anywhere in the world.