Product Overview
Effectively monitor clinical trials from start to finish with Ennov’s comprehensive Clinical Trial Management software.
Each year, clinical trial sponsors search for new ways to improve the efficiency and reduce the costs associated with running their trials. Investigational site efficiency and productivity can be improved by centralizing information, actively monitoring progress, automating schedules, managing finances, and providing accurate reporting and metrics. With the Ennov CTMS, trial sponsors and CROs are able to actively address all aspects of trial management from a single platform: investigator sites, patients, SAEs, deviations, inclusions, visit reports, phone contacts, investigational product management, trial facilities, and finances. Study managers can plan and track their trials in real time to make better decisions faster. With the Ennov CTMS dashboard functionality, study personnel get on-demand analytics to improve quality, control risk, and reduce costs.
Deployment
- Web based
- Cloud Hosted
Pricing
- Subscription
- License Fee
More Information
The Clinical Trial Management Challenge
Each year the Life Sciences companies look for new ways to improve the efficiency and reduce the costs associated with running clinical trials. However, there are many obstacles that can prevent them from achieving their goal. Probably the most significant obstacle they must overcome is the effective selection, monitoring and management of investigational sites.
These companies recognize that site efficiency and productivity can be improved by centralizing information, providing recruitment and screening tools, automating scheduling, managing finances, and providing accurate reporting and metrics. These challenges can be met using Clinical Trial Management software (CTMS), which serves as a single authoritative source for operational data related to the planning, management and reporting of clinical trials.
A Single Authoritative Source for Clinical Trial Information
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.
Centralized and Globally Accessible CTMS Software
Ennov CTMS is built upon the Ennov Compliance Platform (Ennov Process, Ennov Doc and Ennov Report) and leverages that power and flexibility to provide a centralized, 100% web-based solution that can be accessed by clinical teams from any place at any time. Configurable security rules control user access while proving robust collaborative capabilities to internal team members and external partners.
Ennov CTMS is fully integrated with Ennov Clinical Data Management applications. Study information from Ennov EDC can be directly imported into Ennov CTMS to accelerate study startup and eliminate the need for redundant data entry. This approach of consolidating clinical trial data into a single repository gives the trial manager a competitive decision making advantage while improving data quality and consistency.
About the company
Headquartered in Paris, with offices in the US, UK, and Asia, Ennov provides the most original, comprehensive and cost-effective suite of software solutions for the Life Sciences industry. From leading pharmaceutical companies to emerging biotechs, we proudly serve over 250 companies and 250,000 users around the world.
For more than 20 years, we have been developing innovative, powerful and easy-to-use software for regulated content, data and process management. Our solutions are designed and built to support the entire Life Sciences R&D continuum including Clinical, Regulatory, Quality, Pharmacovigilance and Commercial. Ennov is ISO9001:2015 certified for all software products and processes and we boast a 100% success rate in customer audits.
Our solutions enjoy extremely high user adoption rates, thanks to our intuitive user interfaces and commitment to building solutions that work the way our users work. We also have very high customer satisfaction ratings with an on-time project delivery rate of 98.5% and an annual maintenance renewal rate of 96%.