Accelerate Drug Development

Reduce your timelines with our purpose-built AI platform for regulated assays

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About Alchemi

About Alchemi

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.

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Report

Tired of spending hours drafting reports and formatting data tables? Our platform transforms your files into regulatory compliant documents in seconds.

Explore

Report

Tired of spending hours drafting reports and formatting data tables? Our platform transforms your files into regulatory compliant documents in seconds.

Explore

Review

Our AI streamlines QC / QA review by automatically flagging compliance with key guidelines, study-specific criteria, and internal SOPs.

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Review

Our AI streamlines QC / QA review by automatically flagging compliance with key guidelines, study-specific criteria, and internal SOPs.

Explore

Review

Our AI streamlines QC / QA review by automatically flagging compliance with key guidelines, study-specific criteria, and internal SOPs.

Explore

Review

Our AI streamlines QC / QA review by automatically flagging compliance with key guidelines, study-specific criteria, and internal SOPs.

Explore

Review

Our AI streamlines QC / QA review by automatically flagging compliance with key guidelines, study-specific criteria, and internal SOPs.

Explore

Use Cases

Our platform supports you from Method Development to Sample Analysis, covering all major assay types, including PK/PD, Biomarkers, Immunogenicity, and Toxicokinetics.

Use Cases

Our platform supports you from Method Development to Sample Analysis, covering all major assay types, including PK/PD, Biomarkers, Immunogenicity, and Toxicokinetics.

Collaborate

Secure document storage with smart analysis capabilities.

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Collaborate

Secure document storage with smart analysis capabilities.

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Use Cases

Our platform supports you from Method Development to Sample Analysis, covering all major assay types, including PK/PD, Biomarkers, Immunogenicity, and Toxicokinetics.

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

Status Quo

Manual Reporting

Scientists spend up to 30% of their time on manual data processing and report writing

Scientists spend up to 30% of their time on manual data processing and report writing

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

Manual data transfers coupled with manual QC/QA are significant risk factors that can impact quality

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

Sponsors frustrated by mistakes and long turnaround times

Sponsors frustrated by mistakes and long turnaround times

Automated Reporting

Scientist productivity improved through automated report writing (up to 90%)

Scientist productivity improved through automated report writing (up to 90%)

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

LIMs integration removes touchpoints, while AI assisted review allows a risk based approach to quality

LIMs integration removes touchpoints, while AI assisted review allows a risk based approach to quality

Sponsor Satisfaction

Sponsors receive high-quality, validated data sooner

Sponsors receive high-quality, validated data sooner

Sponsors receive high-quality, validated data sooner

75%

Improvement in report turnaround time

100%

Reduction in manual transcription errors

>$4M

Annual time savings in USD dollar value

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Purpose-built AI

Designed for the unique demands of your workflows, ensuring unparalleled speed and accuracy

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Seamless integration

Connect directly to your LIMs + ELN, reducing manual data transformation

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Compliance and Security

Built for compliance with FDA 21 CFR Part 11 and designed to operate in a GxP environment. Our platform also features best-in-class security architecture (SOC 2) and gives you complete control of your data (zero data retention by AI models).

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