AimwellBio Grading System · v1.0

The industry standard for verified intelligence.

Our proprietary 7-point grading system evaluates the confidence, impact, and reliability of every biopharma signal — so you can decide with certainty. Every grade is evidence-backed, source-traced, and audit-ready.

Signal
Ingest the world.
Validation
Verify with rigor.
Decision
Act with confidence.
The AimwellBio Grade Scale

Seven grades. One standard.

Each grade is the result of multi-layer analysis across seven dimensions. The result is a single character — G1 through G7 — that any analyst, regulator, or board member can act on in seconds.

G1
Critical Risk
Severe risk · action required immediately
G2
High Risk
High risk · immediate attention
G3
Elevated Risk
Moderate risk · closely monitor
G4
Neutral
Balanced · no material impact detected
G5
Positive
Favorable signal · monitor opportunity
G6
Highly Positive
Strong positive indicator · act strategically
G7
Very High Confidence
Near-certain outcome · high conviction
← Increasing Risk Neutral Increasing Opportunity →
How grades are determined

Seven dimensions of analysis.

Every grade is the result of a multi-layer evaluation across the dimensions that actually predict regulatory, clinical, and financial outcomes. No vibes. No black boxes.

i · 01
Regulatory Impact
FDA / EMA / global agency posture, guidance trajectory, AdComm signal.
i · 02
Clinical Impact
Endpoint quality, effect size, patient population, comparator strength.
i · 03
Financial Impact
Run-rate exposure, market repricing potential, capital allocation consequence.
i · 04
Data Reliability
Study design rigor, replication, sample size, conflict of interest exposure.
i · 05
Source Quality
Primary vs. secondary, peer review, regulator-grade vs. press-release-grade.
i · 06
Signal Consensus
Cross-source agreement — PubMed, ClinicalTrials.gov, FDA, SEC, EMA.
i · 07
Time Sensitivity
How fast the underlying signal is decaying or compounding.
Every grade. Every time.

Backed. Traced. Audit-ready.

Backed by evidence
Every G-grade points to the underlying signals, studies, and filings. Click through to the source on demand.
Source-traced
Each driver carries its citation. Failed citation resolution automatically downgrades the grade — no exceptions.
Audit-ready
Each grade ships with a tamper-evident signature. Bring our verdicts into a board pack, an FDA filing, an IC memo — they hold up.
Example output

What a grade looks like.

This is the report header a member sees on every graded signal. Same artifact, whether you're reviewing one entity or scanning a thousand.

AimwellBio
SIG-2026-05-12-7421
G2
High Risk
Confidence: 87%
High regulatory and clinical impact detected.
  • FDA guidance change
  • Safety signal escalation
Programmatic access

Wire your stack to the grade.

Pull graded intelligence directly into dashboards, IC memos, regulatory submissions, or downstream agents. One endpoint. One contract. Stable schema.

// GET https://api.aimwellbio.com/v1/intelligence/grade Authorization: Bearer {your_api_key} Content-Type: application/json // Sample response { "signal_id": "SIG-2026-05-12-7421", "grade": "G2", "grade_label": "HIGH RISK", "confidence_score": 0.87, "impact_summary": "High regulatory and clinical impact detected.", "drivers": ["FDA guidance change", "Safety signal escalation"], "dimensions": { "regulatory_impact": 0.92, "clinical_impact": 0.85, "financial_impact": 0.78, "data_reliability": 0.90, "source_quality": 0.88, "signal_consensus": 0.83, "time_sensitivity": 0.91 }, "evidence_count": 24, "sources": ["FDA.gov", "ClinicalTrials.gov", "EMA.europa.eu"], "timestamp": "2026-05-12T14:32:11Z", "aimwell_signature": "A1B7F9…E3C2" }

Endpoint scheduled for member release. Founding contributors receive early API access · request access.

Decide with certainty.

Every signal. Every grade. Every time — backed by evidence, source-traced, audit-ready.