MainEDC™ ePRO Demo play online

For demonstration purposes only
Application for data collection by Subjects of clinical trials (diaries, questionnaires, etc), as well as marketing and feasibility surveys.

The system is validated, compliant with international regulations FDA Title 21 Part 11, GAMP 5, GDPR and supports the CDISC standards.

Full integration with the MainEDC platform facilitates immediate access of Investigators and Study Sponsor to the data collected.
API is available for quick and easy integration with external software, including wearables.

AI technologies ensure instant coding of Subject-reported terms with built-in medical coding dictionaries WHODrug, MedDRA, ATC, ICD.
SMS/ Push/ E-mail notifications make your data most contemporaneous.

Join the community of our system users that goes beyond tens of thousands now!

Always at your service: [email protected]