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New: Protocol Risk Review Sprint — Book a call to reduce preclinical-to-IND risk.

Reduce costly preclinical-to-IND mistakes before studies run

Independent protocol and PK/PD dosing plan risk review for biotech and translational teams. Get clarity and confidence before you execute.

Why PK/PD (not just dose range) matters →

Accelerate your roadmap

Aquarius gives biotech and translational teams an independent review so you can ship protocol and dosing decisions in record time—with fewer surprises at IND or in the clinic.

Without Aquarius

Lower quality protocol decisions, significant rework, and a long tail of edge cases discovered late.

Rework

Often significant

Risk detection

Often late

With Aquarius

Clearer dosing rationale, fewer protocol amendments, and earlier risk detection—independent review before you lock the plan.

Rework

Less

Risk detection

Earlier

Outcomes vary by project; we focus on clarity, fewer amendments, and earlier risk detection.

What we offer

Protocol & PK/PD risk review

Independent review of your protocol and dosing plan before studies run. Identify gaps, assumptions, and regulatory risks so you can fix them early—not at the agency or in the clinic.

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CRO-readiness & alignment

Ensure CRO-facing protocols, timelines, and data expectations are clear and aligned. Reduce rework and miscommunication.

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DDQ and accuracy focus

Due diligence support for investors and teams who need a concise memo on protocol and PK/PD risk—with a focus on accuracy you can ship on.

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Turn your protocol into high-confidence decisions

Book a Call

Trusted by biotech and translational teams

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