Clarity for complex clinical protocols.

Ilana is an AI-powered Microsoft Word add-in that helps researchers identify ambiguity, compliance gaps, and clarity issues—while they write.

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WebelieveAIshould

makecomplexworkeasier—notmorecomplicated.

Ilanahelpsclinicalresearchersidentifyclarityandcomplianceissuesinprotocolswhiletheywrite,

directlyinsideMicrosoftWord.

Byhighlightingpotentialproblemsearly,Ilanasupportsbetter

decision-making,clearercommunication,andmoreefficientstudies—withoutreplacingexpertjudgment.

AIthatworksalongsideresearchers,notaroundthem.

WebelieveAIshould

makecomplexworkeasier—notmorecomplicated.

Ilanahelpsclinicalresearchersidentifyclarityandcomplianceissuesinprotocolswhiletheywrite,

directlyinsideMicrosoftWord.

Byhighlightingpotentialproblemsearly,Ilanasupportsbetter

decision-making,clearercommunication,andmoreefficientstudies—withoutreplacingexpertjudgment.

AIthatworksalongsideresearchers,notaroundthem.

WebelieveAIshould

makecomplexworkeasier—notmorecomplicated.

Ilanahelpsclinicalresearchersidentifyclarityandcomplianceissuesinprotocolswhiletheywrite,

directlyinsideMicrosoftWord.

Byhighlightingpotentialproblemsearly,Ilanasupportsbetter

decision-making,clearercommunication,andmoreefficientstudies—withoutreplacingexpertjudgment.

AIthatworksalongsideresearchers,notaroundthem.

The core of smarter innovation

AI-Powered Analysis

Get instant feedback on your clinical trial protocols. Our AI identifies regulatory gaps, unclear language, and compliance issues so you can submit with confidence.

Get started

AI-Powered Analysis

Get instant feedback on your clinical trial protocols. Our AI identifies regulatory gaps, unclear language, and compliance issues so you can submit with confidence.

Get started

AI-Powered Analysis

Get instant feedback on your clinical trial protocols. Our AI identifies regulatory gaps, unclear language, and compliance issues so you can submit with confidence.

Get started

Regulatory Intelligence

Leverage insights from FDA guidance, ICH guidelines, and thousands of approved protocols to ensure your documents meet the latest regulatory standards.

Get started

Regulatory Intelligence

Leverage insights from FDA guidance, ICH guidelines, and thousands of approved protocols to ensure your documents meet the latest regulatory standards.

Get started

Regulatory Intelligence

Leverage insights from FDA guidance, ICH guidelines, and thousands of approved protocols to ensure your documents meet the latest regulatory standards.

Get started

Seamless Integration

Works directly in Microsoft Word where you write. Review suggestions, accept changes, and improve your protocols without switching applications.

Get started

Seamless Integration

Works directly in Microsoft Word where you write. Review suggestions, accept changes, and improve your protocols without switching applications.

Get started

Seamless Integration

Works directly in Microsoft Word where you write. Review suggestions, accept changes, and improve your protocols without switching applications.

Get started

Accelerate your path to regulatory approval

Faster Protocol Development

Reduce review cycles by catching issues early. Get AI-powered feedback in seconds, not days.

Faster Protocol Development

Reduce review cycles by catching issues early. Get AI-powered feedback in seconds, not days.

Faster Protocol Development

Reduce review cycles by catching issues early. Get AI-powered feedback in seconds, not days.

Fewer FDA Queries

Identify regulatory gaps before submission. Align your language with FDA expectations and ICH guidelines.

Fewer FDA Queries

Identify regulatory gaps before submission. Align your language with FDA expectations and ICH guidelines.

Fewer FDA Queries

Identify regulatory gaps before submission. Align your language with FDA expectations and ICH guidelines.

Consistent Quality

Ensure every protocol meets the same high standards. Standardize terminology and formatting across your team.

Consistent Quality

Ensure every protocol meets the same high standards. Standardize terminology and formatting across your team.

Consistent Quality

Ensure every protocol meets the same high standards. Standardize terminology and formatting across your team.

Evidence-Based Suggestions

Every recommendation cites FDA guidance or industry best practices. Understand the "why" behind each change.

Evidence-Based Suggestions

Every recommendation cites FDA guidance or industry best practices. Understand the "why" behind each change.

Evidence-Based Suggestions

Every recommendation cites FDA guidance or industry best practices. Understand the "why" behind each change.

21 CFR Part 11 Compliant

Full audit trail for regulatory inspections. Track every suggestion, acceptance, and edit with timestamps.

21 CFR Part 11 Compliant

Full audit trail for regulatory inspections. Track every suggestion, acceptance, and edit with timestamps.

21 CFR Part 11 Compliant

Full audit trail for regulatory inspections. Track every suggestion, acceptance, and edit with timestamps.

Works Where You Write

Seamless Microsoft Word integration. Review and accept suggestions without leaving your document.

Works Where You Write

Seamless Microsoft Word integration. Review and accept suggestions without leaving your document.

Works Where You Write

Seamless Microsoft Word integration. Review and accept suggestions without leaving your document.

Ready to write better protocols?

Get started

Book a Demo