About Panaceon AI

Building the Future of Clinical Trial Protocols

We're on a mission to transform how pharmaceutical and biotech companies create, validate, and manage clinical trial protocolsβ€”reducing time, cost, and compliance risk with AI.

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Compliance Score
97%
40%
Faster Protocols
97%
Compliance Rate
500K+
Trials Indexed
100%
Ripple Detection
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AI Generated
12 sections
The Problem We Solve

Why Panaceon? Because Every Day Counts.

Every day a protocol is delayed, a patient waits. Every amendment that could have been prevented costs six months and $500Kβ€”but more importantly, it means six more months before life-saving treatments reach the people who need them.

68%

of protocols require amendments after trial starts1

The ripple effects:
  • Average 6-month delay per amendment
  • Patient enrollment halted during revisions
  • Competitive advantage lost to faster competitors
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Aglaea Protocol Generator
Create trial-ready protocols 40% faster with AI
Create Smarter Protocols β†’
90%

of amendments are preventable compliance issues2

The preventable truth:
  • Missing dose modification criteria
  • Incomplete eligibility requirements
  • Outdated consent language
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Hygeia Compliance Checker
Catches 97% of compliance issues before you submit
Check Compliance Now β†’
$500K

average cost per amendment + 6 month delays

Small changes create big problems:
  • Re-training 50+ study sites
  • Updated consents for 200+ patients
  • Emergency IRB reviews at every site
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Iaso Amendment Tracker
See ripple effects BEFORE you make costly changes
Predict Impact First β†’
$30B

wasted annually on preventable protocol issues3

Industry-wide waste:
  • $18B in amendment costs and delays
  • $8B in failed trials from poor design
  • $4B in regulatory submission rejections
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Aceso Knowledge Base
Learn from 500K trials to build smarter protocols
Explore Knowledge Base β†’
1 Getz et al., 2018. Nature Reviews Drug Discovery Β |Β 2 FDA Critical Path Initiative Report, 2021 Β |Β 3 Tufts Center for the Study of Drug Development, 2023

Our Mission

Clinical trials are the gateway to life-saving treatments. Yet the protocols that govern them are often created using outdated tools and fragmented workflows, leading to costly amendments, regulatory delays, and ultimately, delayed access to medicines for patients who need them most.

Panaceon AI exists to change this. We're building the intelligent protocol development platform that pharmaceutical and biotech companies deserveβ€”one that combines the precision of AI with deep regulatory expertise to create protocols that are right the first time.

The Story Behind Our Name

In Greek mythology, Panacea was the goddess of universal remedyβ€”the cure-all. She was one of five siblings, daughters of Asclepius, the god of medicine. Each sibling represented a different aspect of the healing arts.

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Aglaea
Beauty & Splendor
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Hygeia
Prevention & Health
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Iaso
Recuperation & Recovery
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Aceso
Healing Process

Just as these siblings worked together to provide complete healthcare in ancient mythology, Panaceon AI brings together four essential toolsβ€”each named after a siblingβ€”that address every stage of protocol development. Together, they create something greater than the sum of their parts: complete protocol excellence.

Built For Your Team

Panaceon AI supports every role in clinical trial protocol development

Medical Writers
Clinical Ops
Regulatory Affairs
Leadership
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Industries We Serve

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Large Pharma

Enterprise-scale protocol management for global trials

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Biotech

Agile protocol development for innovative therapies

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Academic Medical Centers

Research-grade tools for investigator-initiated trials

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CROs

Multi-sponsor protocol support at scale

How We Compare

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Feature
Word + Templates
eClinical Platforms
General AI Tools
Panaceon AI
β€’ Protocol Creation
AI-powered first draft generation
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ICH E6(R3) compliant templates
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Therapeutic area-specific AI training
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Cross-section consistency checks
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β€’ Compliance & Validation
Automated regulatory compliance scoring
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Auto-fix suggestions with guideline citations
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Multi-framework support (FDA, EMA, ICH-GCP)
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21 CFR Part 11 audit trail
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β€’ Knowledge & Intelligence
Regulatory guidance knowledge base
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Semantic search (not just keywords)
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Similar trial protocol lookup
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Auto-pull relevant FDA/EMA guidance
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β€’ Amendment & Lifecycle
Version control with diff tracking
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Amendment impact prediction
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Downstream ripple effect detection
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β€’ Team & Workflow
Real-time collaboration
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Review queue with approval workflows
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Export to DOCX, PDF, Excel
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Ready to Transform Your Protocol Workflow?

Join leading pharma and biotech companies already using Panaceon AI.

Get in Touch