Create Your Protocol
Instantly with Confyde
Design trials from scratch, compare scenarios, and accelerate decisions and execution with Confyde's AI-native platform.
.webp)
....as well as consensus guidelines, earnings transcripts, analyst reports and dozens of other sources, all curated by Confyde.ai.
Harnessing and synthesizing the data you need
.svg)
Design higher-probability trials, accelerate execution and prioritise the right assets with Confyde’s AI-native platform.
Why Confyde?
Our unified platform connects the dots across the entire clinical development lifecycle.
MODULE 01
Design High-Probability Trials
AI-native workflows to draft protocols, compare historical studies, and maintain regulatory alignment from day zero.
AI-powered protocol drafting aligned with FDA/EMA
Automated Target Product Profile (TPP) generation
Similarity search across 500k+ historical trials
.svg)
MODULE 02
Accelerate Trial Execution
Operational intelligence that ranks global sites, models enrollment, and keeps budget scenarios within guardrails.
Global site selection with performance-based ranking
Scenario-based enrollment forecasting & monitoring
AI-powered budgeting and resource planning
.svg)
MODULE 03
Prioritise the Right Assets
Landscape and commercial intelligence to quantify demand, spot whitespace, and align BD on the same evidence base.
Therapy landscape analysis across pipelines & approvals
AI-assisted TPP assessments and competitive benchmarks
Demand & revenue forecasting across scenarios
Don't trust us. Test us.
We are confident we can deliver similar results for your team.
How we accelerate phase 3 investment decisions process from weeks to hours.
Screen sites, find PI contact info, and generate SFQs in an afternoon.
Double the capacity of an asset development team with AI assistants.
Real results, measured in time and cost
How pharma and biotech teams use Confyde to move faster.
Study sites chosen in days, not months
Mid-cap global pharmaceutical company
Before
8–12 weeks
$375k
(CRO fees)
After
2 weeks
cost of seat license
Upload a synopsis. Confyde identifies matched trials, ranks optimal sites, distributes feasibility documents, and generates enrollment forecasts — automatically.
Protocol drafts in weeks, not quarters
Venture-backed biotech
Before
~2 months
$550k
in consulting
After
Eliminated with AI-assisted authoring
Reference library vectorised and indexed. AI drafts each ICH M11 section with citations. Human reviewers approve gate by gate. Output maps directly to USDM — no manual conversion.
Scenario planning a drug's full lifecycle
Publicly-traded hub-and-spoke biotech
Before
Spreadsheets and strategy memos
After
~30%
time savings uncapped upside
Replace static Excel models with dynamic scenario trees. Rapidly assess cost, timelines, and risk across upside, base, and downside cases — and assign NPV-based strategic value to each path.
Comprehensive Capabilities
Everything you need to plan, design, and execute successful trials
AI-Powered Protocol Writing
Automate protocol creation and refinement using AI trained on over 500k trials. Generate full protocol sections in minutes.
Target Product Profile (TPP)
Create comprehensive TPPs based on indication and competitive landscape. Compare against approved products.
PTRS Assessment
Assess the Probability of Technical & Regulatory Success. Identify risk factors to optimise design before execution.
Competitive Intelligence
Use semantic AI search to discover similar trials. Analyse enrolment patterns and success rates.
Ready to transform your clinical trials?
Design higher-probability trials, accelerate execution and prioritise the right assets with Confyde’s AI-native platform.
.webp)
Unifying Clinical, Operational & Commercial Intelligence
with AI to accelerate drug development.
