AI-accelerated protocol creation, feasibility, and alignment.

faster trial preparation

AI-accelerated protocol creation, feasibility, and alignment.

AI-accelerated protocol creation, feasibility, and alignment.

The current situation

Solving AI's Opacity Problem

Clinical teams face an impossible choice: use AI that speeds up processes but can't be explained to regulators, or stick with manual methods that guarantee delays.

70% of trials are delayed

Regulators demand clear justification for every decision

$400K+ per amendment

60% require costly protocol amendments

The new standard

Finally, AI you can actually explain

Aika is the first AI-native platform designed to accelerate clinical trial setup and reduce risk by integrating protocol design, feasibility, and regulatory planning.

Achieve more with Aika

Complete documentation

Every suggestion comes with full justification showing exactly how Aika reached its recommendation. Present your choices to regulators with confidence.

Competitive landscape clarity

See what similar trials are doing, identify gaps in the market, and understand where opportunities exist in your therapeutic area.

Seamless workflow integration

Work the way you always have. Aika enhances your process without requiring new systems or extensive team training.

The impact on your work

Faster patient access

Accelerate your timeline by 3-6 months by eliminating research bottlenecks and designing trials that work from the start.

Cost and time control

Save $500K-$1M+ per trial while dramatically reducing the months typically lost to rework cycles and regulatory delays.

Regulatory confidence

Walk into meetings knowing you can defend every decision with specific evidence from comparable successful trials.

Strategic advantage

Make informed choices in hours, not weeks, while competitors struggle with manual research and internal limitations.

50

seconds is

all Aika needs

seconds is all Aika needs

seconds is all Aika needs

AI-generated first drafts of:

Study Synopsis

Full Protocol

Investigator Brochure (IB) sections

Risk Management Plans, Data Management Plans

Informed Consent Forms (ICFs)

AI-generated first drafts of:

Study Synopsis

Study Synopsis

Informed Consent Forms (ICFs)

Informed Consent Forms (ICFs)

Full Protocol

Full Protocol

Investigator Brochure (IB) sections

Investigator Brochure (IB) sections

Risk Management Plans, Data Management Plans

Risk Management Plans, Data Management Plans

Metric

Speed to first draft protocol

Speed to first draft protocol

Time to finalize the protocol

Time to finalize the protocol

Protocol amendments per trial

Protocol amendments per trial

Cost per amendment

Cost per amendment

Feasibility timeline

Feasibility timeline

The Old Way

2 - 3 weeks

2 - 3 weeks

8 - 12 weeks

8 - 12 weeks

Avg. 3.3

Avg. 3.3

$250K – $450K

$250K – $450K

3 - 4 weeks

3 - 4 weeks

1 - 3 days

1 - 3 days

2 - 4 weeks

2 - 4 weeks

Down to 1.5 or fewer

Down to 1.5 or fewer

30 – 50% reduction

30 – 50% reduction

Less than 1 day

Less than 1 day

Features

All-in-one platform

All-in-one platform

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

AI Chat Assistant

This feature provides chat research capabilities that work across platforms and includes seamless integrations with your other tools.

Protocol Generator

This Feature is a cross-platform tool that uses Chat Research to create AI protocols, supporting regulatory processes with scoring and submission.

Feasibility

This feature is focused on AI-assisted patient recruitment and feasibility.

AI Chat Assistant

This feature provides chat research capabilities that work across platforms and includes seamless integrations with your other tools.

Protocol Generator

This Feature is a cross-platform tool that uses Chat Research to create AI protocols, supporting regulatory processes with scoring and submission.

Feasibility

This feature is focused on AI-assisted patient recruitment and feasibility.

Contract and Budgets

Contract and Budgets

Contract and Budgets

Regulatory

Regulatory

Regulatory

Monitoring

Monitoring

Monitoring

MAA

MAA

MAA

Submission

Submission

Submission

Coming Soon

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

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

@2025 Biorce | All Rights Reserved

@2025 Biorce | All Rights Reserved

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