AI-Powered Project Planning for Pharma & Life Sciences Smarter Planning for Research, Trials, and Regulations
From drug discovery to regulatory approval, Kriyastream helps pharma and life sciences organizations plan R&D, clinical trials, and compliance programs with precision and repeatability.
The Challenges in Pharma & Life Sciences Projects
Pharma and life sciences programs face staggering costs and delays:
The average cost to bring a new drug to market exceeds $2.6B (Tufts).
80% of clinical trials miss enrollment timelines, and 50% face cost overruns.
Each day of trial delay costs between $600K–$8M in lost revenue.
Regulatory compliance consumes 20–30% of trial budgets in documentation and audit prep.
Only 12% of drug candidates entering clinical trials ever reach approval, amplifying the cost of inefficiency.
How Kriyastream Helps Pharma & Life Sciences Teams
Protocol-to-Task Mapping
Translate trial protocols into structured, repeatable task chains for execution.
Clinical Trial Forecasting
Model patient recruitment, site setup, and staffing costs across Phase I–IV studies.
Change Control Workflows
Manage protocol amendments and trial deviations with structured updates.
Regulatory Documentation Support
Generate process-level documentation to support FDA, EMA, or IRB compliance reviews.
Key Benefits for Pharma & Life Sciences Organizations
- Reduce trial delays with accurate, AI-powered planning — cutting planning time by up to 25%.
- Improve cost forecasting accuracy, lowering the risk of overruns by 15–20%.
- Standardize repeatable trial workflows, reducing setup time for new studies by 30% or more.
- Automate compliance documentation, cutting audit prep effort by 40%.
Ensure your R&D and clinical trial programs deliver on time, on budget, and in compliance — powered by AI.
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