Clinical trial site management software

The CTMS software solution from Octalsoft is a collection of eTools that are guaranteed to change the way life science organizations, pharmaceutical, and medical device companies conduct and control clinical trials. Right from site identification to study closeout, the tools empower you with various capabilities to manage all your critical processes with ease and flair. Equipped with a live digital dashboard, the system helps you manage calendars, milestones, deadlines, documents, risk-based monitoring, subjects and financials, all in a scalable feature set. It aims to improve efficiencies in planning, resource management, compliances, risk mitigation, data quality, and work processes while reducing operational expenses and accelerating the trial life cycle. Octalsoft CTMS regularly syncs and aggregates all trial data into a consolidated, centralized database.

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Clinical trial site management software

Content:

• CTMS Software
• Clinical Trial Management Technologies
• Clinical Trial Management System
• Improve Study Outcomes with Clinical Trial Software for CROs
• The Lines Are Blurring Between Clinical Trial Management Software Categories
• Clinical Trial Management Software Companies
• Clinical Trial Management System (CTMS)
• Clinical trial management system
• Clinical Trial Software: Understanding EDC, CTMS, ePRO, RTSM, and Addressing Industry Challenges

CTMS Software

InfoEd Clinical Trials Software links trials to related protocols, grants, contracts, publications, conflict of interest information, and patents with a true clinical trial document management system. Quickly build out the arms, visits, cycles, procedures, and billable events that make up a clinical trial protocol. Track all aspects of recruitment, enrollment, and trial participation, from initial contact to completion or withdrawal.

Capture and manage all trial-related information, correspondence and documentation in a virtual regulatory binder. Call Today For A Demo. Offload The Overload: Clinical Trials Management System InfoEd Clinical Trials Software links trials to related protocols, grants, contracts, publications, conflict of interest information, and patents with a true clinical trial document management system. Request a Demo. Investigators and Coordinators Easily create new protocols in only a few steps Record or link required approvals regulatory approvals, contracts, and more to speed study startup and site activation Track enrollment of participants and their progress throughout the trial Manage and share critical study documents with clinical study software Review accumulating trial data and safety information with our Clinical Trials Software Solutions Manage communication with research team members, monitors, participants, and others Track and manage financial activity associated with the trial using our Clinical Trial Data Software and Clinical Trial Design Software Administrators Report on clinical trials and related financial activity for multiple departments, investigators, trials, and participants Standardize processes across the research enterprise with Electronic Research Administration Software Audit trials to verify compliance with regulatory and institutional requirements.

Quickly configure role-based security to control access to sensitive trial and participant information. We know how to manage clinical trials efficiently and effectively. Clinical research software to customize the trial environment to facilitate compliance and support institution-specific processes. Code and track all details of the protocol Create electronic case report forms.

Manage trials across multiple locations using coordinating center tools. Automatically generate transactions for completed milestones and participant visits.

Record payments and age receivables Build and send invoices using customizable templates. Clinical Trials Document Management System Capture and manage all trial-related information, correspondence and documentation in a virtual regulatory binder.

Share critical study documents with all members of the research team Version uploaded documents. Store and manage documentation related to individual participant. Track site monitoring visits, audits, and routine compliance reviews and their outcomes. Report on recruitment, enrollment, and completion of trial activities.

Clinical Trial Management Technologies

There were press releases posted in the last 24 hours and , in the last days. The system maintains and manages planning, performing and reporting functions, along with participant contact information, tracking deadlines and milestones. Companies are having to conduct multiple clinical trials at the same time. And comply with industry regulations. They need to be able to see and manage their clinical trials effectively so they can improve inefficiencies in the process, and get the data they need.

Clinical Trial Management System

Introducing degrees of performance with optimized, streamlined, and accelerated clinical trial processes. Simplify every aspect of trial journey from start-up to monitoring, analysis, and compliance. A robust clinical trial management system, providing you powered capabilities with simplicity, enabling further speed of site selection and startup, enrollment, and execution and tracking — all while integrating with your other existing systems, to ensure seamless flow of information across your operations. Innovative modern pharmaceuticals often require a deeper understanding of the entire trial life cycle in order to effectively reach the goal of treating and preventing disease. Trials by P is a cloud-based clinical trial management software suite that effectively supports multiple studies across various sites while safeguarding your clinical trial process and data. Comprehensive CTMS solutions allow for successful and secure clinical drug trials through authentic relationships and rich trial lifecycle analytics. Launching a clinical drug trial requires dozens of moving parts to be successful, and managing those parts can be a challenge, even for the most experienced company. Our Powered solutions are tailored to meet your needs — augmenting your existing business processes and integrated with your operational flow. P strives to help pharma and life sciences companies streamline their organizational efficiency and processes through robust IT solutions and pharma software tailored to their unique needs.

Improve Study Outcomes with Clinical Trial Software for CROs

Clinion CTMS is an Integrated Clinical Trial Management Software that allows users real-time visibility across the study spectrum, allowing for real-time interventions and course correction, leading to accelerated study timelines. Customized workflows, pre-set processes, real-time status reports, automated alerts, real-time monitoring, holistic visibility — result in immediate and sustained efficiencies to reduce trial costs significantly. Real-time Integration gives enhanced visibility into all aspects of the clinical trial process - from study plan, design, site selection, subject recruitment, data capture, monitoring, remote monitoring, drug allotment, Inventory management and data management. Moreover, it is constantly evolving, adding new features and modules almost daily, making it more versatile and user-friendly for its users. Enables study project managers to manage studies remotely by setting up milestones and assigning CRAs Clinical Research Associates to studies and sites.

The Lines Are Blurring Between Clinical Trial Management Software Categories

Study managers and CRAs need a simple planning and tracking solution that focuses on monitoring requirements. A mobile-first interface places important actions and information at your fingertips. Practicality — Focused on the simplest, most practical features not on heavy configuration. Service — Backed by a global professional and technical services team with premium support for any requests necessary to succeed. Content and eTMF — Built-in clinical content solution, to create, collaboratively review, approve, and publish to the eTMF archive while providing complete transparency to all tasks, activity, and data with a complete author-to-archive audit trail. Mobile — Designed to be mobile-first, providing a fully-functional Site Visit app, along with existing content management and eTMF mobile experiences.

Clinical Trial Management Software Companies

InfoEd Clinical Trials Software links trials to related protocols, grants, contracts, publications, conflict of interest information, and patents with a true clinical trial document management system. Quickly build out the arms, visits, cycles, procedures, and billable events that make up a clinical trial protocol. Track all aspects of recruitment, enrollment, and trial participation, from initial contact to completion or withdrawal. Capture and manage all trial-related information, correspondence and documentation in a virtual regulatory binder. Call Today For A Demo. Offload The Overload: Clinical Trials Management System InfoEd Clinical Trials Software links trials to related protocols, grants, contracts, publications, conflict of interest information, and patents with a true clinical trial document management system. Request a Demo. Investigators and Coordinators Easily create new protocols in only a few steps Record or link required approvals regulatory approvals, contracts, and more to speed study startup and site activation Track enrollment of participants and their progress throughout the trial Manage and share critical study documents with clinical study software Review accumulating trial data and safety information with our Clinical Trials Software Solutions Manage communication with research team members, monitors, participants, and others Track and manage financial activity associated with the trial using our Clinical Trial Data Software and Clinical Trial Design Software Administrators Report on clinical trials and related financial activity for multiple departments, investigators, trials, and participants Standardize processes across the research enterprise with Electronic Research Administration Software Audit trials to verify compliance with regulatory and institutional requirements.

Clinical Trial Management System (CTMS)

Easily configure every part of our proprietary platform. The system is fully managed by end users. No installation required.

Clinical trial management system

Clinical trials are complex projects, and managing its various aspects is simply too complicated for a typical project management software. Individual applications can do budgets, data collection, compliance, research timelines, and more. However, juggling different platforms that do not seamlessly connect together is inefficient. It is better to have this information all in one place in order to ensure that you will not miss anything. Clinical trial management software covers all these attributes of your research project and more.

Clinical Trial Software: Understanding EDC, CTMS, ePRO, RTSM, and Addressing Industry Challenges

We empower data managers, clinical researchers, and study participants by enabling more efficient clinical research through smart clinical data management and automation. The regulatory support package is robust and validation maintenance is simple and straightforward. Development processes are well controlled and the company is at a mature place in testing and compliance. Aside from really nice software, the people are really lovely and provide excellent support. The web-based interface is user-friendly, and the new features of real-time queries, and auto-saving features really improve the user experience for data entry persons. Specifically the customizability of the forms and events when designing a survey has benefitted us immensely. Additionally, the OpenClinica team members work hard to both understand what their users need and proactively update the software with new features.

Sponsors, CROs, sites and clinical trial vendors work so very hard to make clinical trials successful. This arduous work includes protocol development, regulatory approvals, trial management, vendor selection, site selection, start-up, and effective participant recruitment just to get the study off the ground. But one fact remains consistent today: Study participants, the most valuable part.