Audience
Companies looking for a Clinical Trial Management solution
About MAISi
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.
Other Popular Alternatives & Related Software
EasyTrial
As EasyTrial.net is a web-based system, you can access the study data at any time from any place. Using EasyTrial.net you have the advantage that you can involve others easily as individual access control enables you to share specific data with others and block access to other data if required. EasyTrial.net is a GDPR compliant storage solution. You have 100% control of your data. As the investigator, you are the data holder and EasyTrial.net, the data processor, will enter data handling agreements if requested. As a professional supplier of data security, we are specialists in and highly focused on IT and cyber security. As thousands of clinical trials have been carried out inside EasyTrial.net over the years, the system is security-approved by many data legislation authorities, hospitals and educational institutions in many different countries.
Learn more
SimpleTrials
SimpleTrials is an on-demand, subscription-based Clinical Trial Management System (CTMS) designed for sponsors, Contract Research Organizations (CROs), and investigative sites. It offers a comprehensive suite of tools to effectively plan, manage, and track clinical study portfolios, including features such as site startup and subject tracking, document management with integrated electronic Trial Master File (eTMF), real-time study analytics, calendar and monitoring, custom fields and trackers, ad-hoc reporting, planning and milestones, site contracts and payments, and electronic visit reports. It supports compliance with 21 CFR Part 11 and provides a secure, validated environment for clinical trial data. Users can customize tracking views, integrate with various Electronic Data Capture (EDC) systems, and utilize built-in templates for consistent document management.
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Mosio
Mosio enables research teams to improve subject adherence, communications, and data collection on mobile’s most popular channel: text messaging.
Our software makes research teams more efficient in how they communicate with study participants through messaging automation and interactive elements delivered to participant mobile phones.
WHO WE HELP:
+ Clinical Trial Sponsors (Pharma and Biotech)
+ Cancer Centers and Clinical Research Organizations
+ NIH-Funded Studies
+ Public Health Agencies
+ Clinical Trial Managers, Clinical Operations Managers/Directors, Clinical Project Managers, Principal Investigators, Clinical Research (Study) Coordinators, and any research staff who communicate regularly with study participants.
BENEFITS:
+ Interactive dosing reminders and medication adherence alerts.
+ Automate data collection.
+ Increase engagement and adherence.
+ Fix your no-show problem with SMS appointment reminders.
+ Improve retention with automated check-ins.
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Ennov CTMS
Ennov CTMS facilitates the end-to-end management of clinical trials. The software allows sponsors to be more efficient, to make better decisions, to ensure compliance, to select investigators well, to monitor patient recruitment and to manage finances. Ennov CTMS includes comprehensive directories to manage site personnel (investigators, sub-investigators, study coordinators, pharmacists) and organizations (hospitals, competent authorities, CROs, suppliers).
Ennov CTMS provides functions for tracking patients, patient visits, EDC data, activities, queries, deviations, adverse events, drug supply, monitoring visits and finances. A full complement of reports and dashboards provide total visibility into the status of each study, country, site and investigator to provide the information necessary to make the best decisions possible.
- Comprehensive CTMS software
- Integrated with Ennov Clinical Data Management
- Clear visibility into investigational sites
- Integrated workflow
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Integrations
No integrations listed.
Company Information
Agile Health Computing
Australia
www.agilehealthcomputing.com
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Product Details
Platforms Supported
Windows
Training
Documentation
Live Online
Support
Phone Support
Online
MAISi Product Features
Clinical Trial Management
21 CFR Part 11 Compliance
Document Management
Enrollment Management
HIPAA Compliant
Patient Database
Recruiting Management
Scheduling
Study Planning
Electronic Data Capture
Monitoring
