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Doqboard

Doqboard offers a secure electronic Case Report Form (eCRF) platform designed specifically for observational clinical research, enabling hospitals and research teams to efficiently manage data collection and participant engagement. By facilitating collaboration among healthcare actors, Doqboard enhances the quality and speed of real-world data acquisition for clinical studies.

Mont-Saint-Aignan, FranceFounded 20191500+ followers
Updated 4 months ago

Funding

$250K raised to dateRaised to date based on public sources. This may differ from the amount the company actually raised and is based only on what is publicly available on the internet.

Funding rounds are not available yet.

Founders

Product

Problem

Observational clinical research faces challenges in efficiently managing data collection and participant engagement, often relying on manual processes and disparate systems. This can lead to increased administrative burden, data quality issues, and delays in real-world data acquisition.

Solution

Doqboard offers a secure electronic Case Report Form (eCRF) platform designed to streamline data collection and enhance collaboration in observational clinical research. The platform provides researchers, hospitals, associations, and industry partners with a dedicated interface to manage observational studies, registries, and real-world data. By centralizing data management and facilitating communication among healthcare actors, Doqboard improves the efficiency, quality, and speed of clinical research projects. The platform's collaborative features ensure optimal organization and task distribution, while its investigator-centric design promotes user engagement and project success.

Target Audience

Doqboard serves researchers, hospitals, research associations, and healthcare industries involved in observational clinical research.

Features

  • Tailor-made interface for researchers to conduct observational research and maintain control over their data.
  • Secure tool for hospitals to enable clinical teams to work collectively on research development.
  • Centralized platform for associations to deploy projects safely and optimize member commitment.
  • Dedicated environment for industry partners to engage investigators and obtain quality real-world data on drugs and medical devices.
  • HDH and ISO 27001 certified hosting for secure data storage.
  • Customized management of participant rights to ensure data privacy.
  • Controlled access to data and projects to maintain data integrity.
  • GDPR compliance to meet regulatory requirements.
This profile is AI-generated and may contain inaccuracies.