Six agents. One operating system.

Advanced intelligence for clinical agility

The platform Aika delivers intelligence for clinical trial simulation, protocol, feasibility and execution.

Book a demo

Six agents. One operating system.

Advanced intelligence for clinical agility

The platform Aika delivers intelligence for clinical trial simulation, protocol, feasibility and execution.

Book a demo

Aika, the end-to-end operating system

Aika is a continuous intelligent layer from protocol decision to regulatory submission.

Aika is the first clinical-native operating system that continuously synchronises intelligence across every stage of clinical development, ensuring that decisions made in one workflow automatically inform every downstream activity.

Connect your tools, integrate your systems, and bring your own data, securely.

The clinical trial process

Aika one continuous layer across every phase

Portfolio decision

Study design

Site selection

Negotiation

Budgeting

Regulatory submission

Three intelligences, six agents

Portfolio intelligence

What to develop and why

Simulation

HEOR, development scenarios and risk-adjusted NPV

Design intelligence

How to design the trial

Protocol

Evidence-based protocol generation and scoring

Feasibility

Site selection and patient pool by country

Execution intelligence

How to run and file it

Contracts

Automated CTA redlining and fallback language

Budget

Full multi-country study cost projection

Regulatory

eTMF-ready submission documentation

Aika enables full control over
timelines, budgets, and execution

Aika enables full control over timelines, budgets, and execution

Scientific and clinical excellence

Our team of clinical experts covers all therapeutic areas, co-develops product feature and secures validated and structured data input levels.

Connect your tools, integrate your systems, and bring your own data, securely.

Operational impact analysis

Operational
impact analysis

The Old Way

Protocol (submission ready)

Protocol

(submission ready)

Protocol (submission ready)

Cost per amendment

Value across the trial

The old way

The
Old Way

90 days

$535K

Status quo old way

With Aika

With
Aika

under 30 days

minimized significantly

$100M+ protected with Aika, from Phase 1 to approval

Your
Savings

Your savings

70% faster

$400K avg. savings per amendment

$100M+ protected with Aika, from Phase 1 to approval

$100M+ (due to lower cost, earlier revenues, faster timelines) from Phase 1 to approval]

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No blackbox, traceable outputs only

Aika is a continuous intelligent layer from protocol decision to regulatory submission.

Work faster and smarter with Aika and its purpose-built AI tools for clinical specialists. From benchmarking to final sign-off, Aika ensures every document is explainable, traceable and always under your control.

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Protocol

Simulation

Feasibility

Contracts

Budget

Regulatory filing

All within minutes. Defensible. Connected.

Within minutes, you can generate HEOR and study design simulations, protocols, site selection and feasibility reports, eTMF-ready regulatory documentation and full study cost projections.

GxP-aligned

SOC2 Type II Certified

HIPAA-ready