Accelerate Drug Development
Reduce your timelines with our purpose built AI platform for regulated assays
Built by a team with experience
Report
Tired of spending hours drafting reports and formatting data tables? Our platform transforms your files into regulatory compliant documents in seconds.
Review
Our AI streamlines QC / QA review by automatically flagging compliance with key guidelines, study-specific criteria, and internal SOPs.
Collaborate
Secure document storage with smart analysis capabilities.
Use Cases
Our platform supports you from Method Development to Sample Analysis, covering all major assay types, including PK/PD, Biomarkers, Immunogenicity, and Toxicokinetics.
Automate. Accelerate.
Achieve More with Alchemi
Achieve More with Alchemi
Status Quo
Manual Reporting
Scientists spend up to 30% of their time on manual data processing and report writing
Manual QC/QA
Manual data transfers coupled with manual QC/QA are significant risk factors that can impact quality
Project Delays
Sponsors frustrated by mistakes and long turnaround times
Automated Reporting
Scientist productivity improved through automated report writing (up to 90%)
QC/QA Efficiency
LIMs integration removes touchpoints, while AI assisted review allows a risk based approach to quality
Sponsor Satisfaction
Sponsors receive high-quality, validated data sooner
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How it works
Purpose-built AI
Designed for the unique demands of your workflows, ensuring unparalleled speed and accuracy
Seamless integration
Connect directly to your LIMs + ELN, reducing manual data transformation
Compliance and Security
Built for compliance with FDA 21 CFR Pt 11 and operation in a GxP environment, as well as best in class security architecture (no training on user data, encryption at rest)
75%
Improvement in report turnaround time
100%
Reduction in manual
transcription errors
transcription errors
>$4m
Value of time saved
per year
per year
