Redefining trials.
Reimagining cure.

The first clinical AI platform that speeds up drug development without compromising compliance.

See how it works

Partners with

Redefining trials.
Reimagining cure.

The first clinical AI platform that speeds up drug development without compromising compliance.

See how it works

Partners with

Redefining trials.
Reimagining cure.

The first clinical AI platform that speeds up drug development without compromising compliance.

See how it works

Partners with

AI-accelerated protocol creation, feasibility, and alignment.

70% faster trial preparation

AI-accelerated protocol creation, feasibility, and alignment.

70% faster trial preparation

AI-accelerated protocol creation, feasibility, and alignment.

70% faster trial preparation

AI-accelerated protocol creation, feasibility, and alignment.

$400K+ saved per
avoided amendment

AI-accelerated protocol creation, feasibility, and alignment.

$400K+ saved per
avoided amendment

AI-accelerated protocol creation, feasibility, and alignment.

$400K+ saved per
avoided amendment

AI-accelerated protocol creation, feasibility, and alignment.

Feasibility analysis in
seconds, not weeks

AI-accelerated protocol creation, feasibility, and alignment.

Feasibility analysis in
seconds, not weeks

AI-accelerated protocol creation, feasibility, and alignment.

Feasibility analysis in
seconds, not weeks

AI-accelerated protocol creation, feasibility, and alignment.

Up to 50% fewer
protocol amendments

AI-accelerated protocol creation, feasibility, and alignment.

Up to 50% fewer
protocol amendments

AI-accelerated protocol creation, feasibility, and alignment.

3-6 months faster
patient access

AI-accelerated protocol creation, feasibility, and alignment.

3-6 months faster
patient access

AI-accelerated protocol creation, feasibility, and alignment.

3-6 months faster
patient access

Build compliant-by-default studies for global submissions.

Designed to meet
FDA, EMA & PMDA

Build compliant-by-default studies for global submissions.

Designed to meet
FDA, EMA & PMDA

Build compliant-by-default studies for global submissions.

Designed to meet
FDA, EMA & PMDA

AI-accelerated protocol creation, feasibility, and alignment.

Up to 50% fewer
protocol amendments

AI-accelerated protocol creation, feasibility, and alignment.

Up to 50% fewer
protocol amendments

Smarter. Faster. Intuitive.

Meet Aika

The new standard for clinical trials

Aika is the first AI-native platform for clinical trials, built to streamline protocol design, feasibility, and regulatory planning in one intuitive workspace. It helps clinical teams accelerate trial setup, reduce risk, and bring treatments to patients faster.

The problem with AI in clinical trials?

The problem with AI in clinical trials?

Nobody can explain how it works.

Nobody can explain how it works.

Nobody can explain how it works.

Features

All-in-one platform

All-in-one platform

All-in-one platform

Each Aika feature is purpose-built to solve a core clinical trial challenge.

Explore Aika

Explore Aika

Explore Aika

Testimonials

Trusted by Leaders. Backed by Science.

Trained on 560,000+ clinical trials.

“Biorce is exactly the kind of pioneering company we’re here to back. They’re combining deep sector expertise with cutting-edge AI to solve what truly matters. Their platform has the potential to radically reduce both the time and cost of bringing new treatments to market, unlocking huge value for pharma and, more importantly, faster access to life-saving therapies for patients.”

Tove Larsson

General Partner | Norrsken VC

Used across US, EU & APAC by global clinical trial teams.

"The expansive potential of Jarvis hints at a wealth of untapped applications beyond drugs development; it opens the door to evolutionary possibilities that could help redefine efficiency and precision in the broader medical field"

Ricardo Matias

CRIO | Co-Founder of Kinetikos

Built by former CRO, clinicians, regulatory, and AI leaders.

$5M invested by Norrsken, Europe’s leading impact VC to reinvent clinical trials.

"I think this is a fantastic tool for clinical trialists that will not only save time but could potentially reduce the number of avoidable protocol amendments, saving costs and enhancing confidence in evaluation of the study objectives"

Laurence Skillern

Medical Director | CMO of ISTESSO

Medical Director | CMO of ISTESSO

Medical Director | CMO of ISTESSO

Ready to accelerate your next clinical trial?

Book a demo

Ready to accelerate your
next clinical trial?

Book a demo

Ready to accelerate your
next clinical trial?

Book a demo

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