Self Reporting Clinical Trial Health Report

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  Overview

Inspiration

Clinical trials often face challenges with consistent and timely reporting of adverse events. We wanted to create a simple, accessible tool to empower patients and healthcare professionals to log their health updates regularly — improving transparency, safety, and communication in the pharmacovigilance process.

What it does

The tool allows patients and HCPs (Healthcare Professionals) to easily submit reports on adverse drug reactions and overall health status during clinical trials. The data is structured and sent directly to pharma companies or research systems for monitoring and analysis.

How we built it

Bolt and Netlify

Challenges we ran into

Ensuring medical terminology was both accurate and patient-friendly Structuring the report data in a format that's useful for pharma companies Managing data privacy and secure submission processes

Accomplishments that we're proud of

Built a working prototype with end-to-end reporting in under 20 minutes Created a clean, user-friendly interface usable by both patients and HCPs Simulated realistic data structures that can plug into clinical trial reporting systems

What's next for Self Reporting Clinical Trial Health Report

Integrate with EHR systems and pharma company databases Add multi-language support for broader accessibility Implement AI-based adverse event analysis and alerts Ensure compliance with HIPAA and GDPR for data security

Built With

• bolt
• netlify