Solutions & Services
MainEDC™ ePRO - Patient e-Diary
Try the new MainEDC™ ePRO in decentralized and traditional clinical trials of all phases, pharmacovigilance source data capture, patient registries, marketing and feasibility studies. The system is accessible via mobile apps for iOS and Android or via a web-adapted page without installation.
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.
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.
Instantly induce high customer loyalty to your brand name. Demonstrate to your clinical trial subjects and postmarketing research audience that you:
Invite your customers / study subjects to the web page or mobile app published under your company brand name.
The system supports electronic sign-off of informed consent, personal data processing and technical agreements.
Contact your customers directly, form your target audience, and use the collected data for new markets access. MainEDC™ ePRO will process up to 60 marketing indicators automatically:
Adjust subjects schedule flexibly and manage their access on your own or by delegating this to investigators.
MainEDC™ ePRO supports even most sophisticated workflows in access granting, schedule configuration, reminding of questionnaire completion, etc
MainEDC™ ePRO shares the platform with EDC, IWRS and Drug Supply components of MainEDC™, also supporting the MainEDC™ Hi Load technology for larger studies.
The platform has successfully passed benchmark testing and, what is even more valuable, its high scalability has been proven by real practical use in several clinical studies enrolling up to 70,000 subjects each.
Rebranding / white-labeling
for cell phone apps,
mobile and desktop website
All MainEDC™ Data Management / Data Science
functionality is available,
including export to all formats
Subject self-registration for clinical trials,
feasibility studies, marketing programs
and patient registries
Quick and easy adding subjects
from investigator interface
(SMS / email)
Immediate access to collected data
from investigator and site team interfaces
Compliance with 21 CFR part 11,
Support for up to 100 000 subjects
within a single project
Integration with wearable devices
(fitness trackers, smart watches)
Export to CDISC SDTM,
SAS, XML, XLS, and Module
Built-in medical coding
WHODrug, MedDRA, ATC, and ICD
for external integrations
|Basic||Pro||Pro Plus||Enterprise||Enterprise Plus||VIP|
|Pricing per study per month||$ 999||$ 1,499||$ 1,999||$ 2,499||$ 2,999||$ 4,999|
|MainEDC™ ePRO Platform|
|Number of surveys||< 20||< 50||Unlimited||Unlimited||Unlimited||Unlimited|
|Number of subjects||< 50||< 300||< 1,000||< 2,500||< 5,000||10,000+|
Have you got any questions? Please feel free to reach out