AI-Powered Clinical Trial Intelligence for the Life Sciences Industry

PathwayIQ understands protocols, reviews submissions, and flags issues. Allow your clinical trial managers to focus on what matters.

Existing Solutions Aren't Built For Speed.

You log into a clunky system. You see dozens of new case report form submissions, each with different formats. Each one needs review. Each one could have compliance issues. Each one is a potential delay.

Manual File Retrieval

Case report form submissions have to be manually retrieved by clincial trial managers, creating toil and bottlenecks.

Inconsistent Data Formats

Every trial site does things differently. Some use structured data. Others write everything in free-form notes.

Fragmented and Siloed Systems

Data is scattered across different systems, making it difficult to track and review.

Outdated software and manual workflows are costing you time and money.

Clinical trial timelines are stretched out and delayed.

Every day of delay costs thousands in operational overhead and lost opportunity. Manual review processes mean issues aren't caught until weeks later, forcing protocol amendments, site corrections, and regulatory re-submissions that push timelines further out.

Clinical trial managers waste time on manual review.

Hours spent reading through case report forms line by line, cross-referencing protocols, and hunting for inconsistencies. This repetitive work prevents managers from focusing on strategic decisions, site relationships, and trial optimization—the work that actually moves trials forward.

Life sciences companies spend more on running clinical trials.

Inefficient workflows require larger teams, longer timelines, and more resources. The cost of manual review, delayed issue detection, and extended trial durations compounds into millions in unnecessary spending that could be invested in innovation instead.

Meet PathwayIQ: Your New AI Copilot for Clinical Trial Management

Our case report agent understands your clinical trial protocols like, reviews submissions, and identifies data quality issues.

Protocol Intelligence

Upload your clinical trial protocols once. PathwayIQ will understand requirements and automatically generate data quality rules for case report form submissions.

Instant Review

Our agent will automatically review case report form submissions against clinical trial protocols, cross-referencing submissions against protocol requirements and data quality rules.

Aggregated Insights

PathwayIQ aggregates insights from case report form submissions, allowing clinical trial managers to see the overall performance of their case report form submissions and identify trends.

From Chaos to Clarity

PathwayIQ helps clincial trial managers review case reports more efficiently, search information, and make better decisions.

Review Case Reports in Minutes

Fix Issues Before They Escalate

Instantly Search And Aggregate Information

Ready to Transform Your Case Report Review Workflow?

Join the clinical trial managers who've reclaimed their time and improved their efficiency.