✨ AI Summary
Harbor is an AI-enabled system of record that replaces legacy electronic data capture (EDC) systems for clinical trials. It automates study setup from protocols and extracts data directly from uploaded source documents, eliminating manual data entry.
Best For
Medical device companies running clinical trials, Pharmaceutical companies conducting clinical research, Clinical research sites and coordinators
Why It Matters
It dramatically reduces clinical trial setup time and operational costs by automating data capture and eliminating error-prone manual entry.
Key Features
- Automatically configures clinical trial databases by reading protocols
- Extracts data directly from uploaded source documents using AI
- Eliminates manual data entry for research site coordinators
- Maintains full regulatory compliance with GCP and 21 CFR Part 11
Use Cases
- A clinical research coordinator at a busy oncology site uploads patient lab reports and visit notes directly into Harbor instead of manually transcribing each data point into a legacy EDC system. This saves them over an hour per patient visit and reduces transcription errors that previously triggered weeks of query resolution.
- A data manager at a mid-sized pharmaceutical company uses Harbor's protocol-reading AI to automatically generate the study database structure for their Phase II trial. This eliminates the two-month configuration process with their previous EDC vendor, allowing them to launch patient enrollment ahead of schedule.
- A medical device startup's regulatory lead monitors trial data quality in Harbor's dashboard, where AI flags potential inconsistencies in source documents for immediate review. This proactive approach replaces the traditional reactive query cycle, ensuring cleaner data for their FDA submission.