Product Overview
- Electronic informed consent (e-Consent)
- Decentralized and classical clinical trials of all phases
- Data collection from medical devices
- Pharmacovigilance source data capture
- Laboratory trials
- Registries, marketing and feasibility, projects clinical, drug safety, and marketing data
Leverage your individual, flexibly configurable one-stop shop for simultaneous collection of clinical, drug safety and marketing data.
The system utilizes subject self-registration with or without the access approval step, which is not only time-saving but also allows to expand drastically the search for potentially eligible subjects, even bypassing clinical sites. Intuitive interfaces, good usability ensure users comfort and speed while entering data. MainEDC™ ePRO is fully integrated with the rest of the MainEDC™ platform but it can be used independently, too.
Deployment
- Web based
- Cloud Hosted
Pricing
- Subscription
- License Fee
More Information
- Handle decentralized trials in a most advanced way
- Provide good customer care
- Value the feedback
- Comply with regulatory requirements
Apply your branding to the platform by labeling both applications at one go (mobile app and web-adapted page) with your logo and style. You can publish the app in the Apple Store and Google App Market under your company name.
About the company
Data Management 365 is a software firm with deep expertise in clinical trials. We emphasize robust skills in Clinical Data Management and Data Science, enabling us to address Data Managers’ challenges, enhance our MainEDC™ platform through real-time feedback, and share best practices with clients. This expertise also aids communication with Clinical Data Management professionals. We originated as a spin-off from Flex Databases and were founded by IT experts, doctors, and researchers experienced in clinical trials. Thus, we intimately understand and cater to Data Management Software needs using cutting-edge tech.
