01 | Decide
Portfolio & Strategy
Portfolio and strategy modules covering the competitive landscape, real-world evidence, and commercial access outlook.
02 | Design
Study Activation
Study activation modules covering protocol simulation, feasibility assessment, contract negotiation, budget negotiation, and site activation.
03 | Deliver
Execution
Execution modules to drive a trial through completion, including data and connectivity, risk-based oversight, patient eligibility, site management, and regulatory submissions.
01
Portfolio
02
RFP
03
Study design
04
Site start-up
05
Study conduct
06
Submission
Aika proposes, your team decides.
Scientific and clinical rationale
Our team of clinical experts covers all therapeutic areas, co-develops product features, and ensures access to validated, structured scientific and regulatory data. Connect your tools, integrate your systems, and securely bring your own data.
Let's connect
Operational impact analysis
Baseline
The old way
Protocol (submission ready)
90 days
Cost per amendment
up to $535K
Value across the trial
Status quo old way
Intelligent layer
With Aika
Protocol (submission ready)
under 30 days
Cost per amendment
minimized significantly
Value across the trial
$100M+ protected Phase 1 to approval
Net return
Your savings
Protocol (submission ready)
70% faster
Cost per amendment
$400K avg. savings per amendment
Value across the trial
full lifecycle covered
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Costs
Recover time and capture more value. Reduce costs, manual effort, and rework while increasing productivity and delivering a measurable return on investment.
Cascade
Change one thing, everything updates. When a change is made to the protocol in Aika, the platform reasons across every connected document, updating them for your review and approval.
Compliance
Trusted intelligence. Stronger compliance. Aika supports regulatory confidence with evidence-backed, fully traceable outputs and continuous compliance monitoring.
Key clinical documents and reports
Within minutes, you can generate core clinical trial documents (protocol, IB, ICF), HEOR and study design simulations, site selection and feasibility reports, eTMF-ready regulatory documentation and full study cost projections.
Aika covers it all
The clinical operating system represents a new way of working across the entire clinical trial lifecycle.
