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Miracle

Miracle provides a unified dashboard that integrates data from various clinical trial platforms and vendors, enabling real-time analytics and visualization of recruitment and performance metrics. This technology helps clinical operations identify bottlenecks and enhance efficiency, allowing trials to be completed faster and with greater transparency.

San Francisco, United StatesFounded 202249700+ followers
Updated 20 months ago

Funding

$500K 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.

NS
Funding rounds are not available yet.

Founders

Product

Problem

Clinical trials often suffer from a lack of real-time visibility into key performance indicators, leading to delays, inefficiencies, and difficulties in identifying bottlenecks. Data is often scattered across multiple platforms and tracked manually via spreadsheets, hindering timely decision-making and proactive intervention.

Solution

Miracle offers a unified, real-time dashboard that integrates data from disparate clinical trial platforms, such as EDC, IRT/RTSM, lab systems, and study websites, providing clinical operations teams with comprehensive visibility into trial performance. The platform automates data aggregation and harmonization, enabling interactive visualizations and drill-down capabilities to uncover bottlenecks and trends by site and over time. By centralizing data and providing real-time insights, Miracle empowers teams to make data-driven decisions, optimize site performance, and accelerate clinical trial timelines. The platform also facilitates continuous data cleaning, safety monitoring, and patient profile review, enhancing data quality and patient safety.

Target Audience

Miracle is designed for clinical operations teams, data scientists, and clinical trial managers within pharmaceutical, biotechnology, and medical device companies, as well as CROs managing clinical trials.

Features

  • Ready connectors for integration with common clinical trial platforms (EDC, IRT/RTSM, lab systems, study websites)
  • Automated data integration and harmonization from various sources
  • Interactive, unified dashboard with real-time visualizations and drill-down capabilities
  • AI-powered enrollment projections and scenario planning
  • Continuous data cleaning and review functionalities
  • Safety monitoring tools for adverse event analysis
  • Patient profiles with integrated data from EDC, safety databases, and lab systems
  • Role-based access control and audit trails for data security and compliance (SOC II, HIPAA, GDPR)
This profile is AI-generated and may contain inaccuracies.