Now Available to All Members

Introducing
ResearchNexo IQ

"One system that turns authoritative health data into cited, auditable deliverables."

Medinexo's new AI research and intelligence engine — purpose-built for clinical research. State a task in plain language. A coordinated team of AI specialists queries 50+ authoritative data sources in parallel and returns a structured, cited deliverable you can trace back to the source.

Discover more
50+Authoritative data sources
30+AI specialists
20+Radar boards
95–97%Citation fidelity
Exclusive Member Offer

Your Credits Are Waiting

As a valued Medinexo member, you receive complimentary ResearchNexo IQ credits from day one — included automatically with your membership, no extra sign-up required.

650
First-Month Credits

First-Month Launch Bonus

Your first month includes 500 launch bonus credits plus your standard 150 monthly credits — 650 total to explore the full depth of ResearchNexo IQ at no additional cost.

150
Monthly Credits

Ongoing Monthly Allowance

Starting month two, your membership automatically includes 150 ResearchNexo IQ credits renewed each month — at no additional charge.

Simple by design

How ResearchNexo IQ Works

You state a task in plain language. The system assembles the right AI specialists, runs them in parallel across dedicated data sources, and hands back a business-ready deliverable — cited and auditable to the source.

1

State a Task

Describe what you need in plain language — e.g. "PubMed-backed claims dossier for ashwagandha for sleep."

2

Task Manager

An AI task manager reads your request and assembles the right team of specialists for the job.

3

Specialists Run

Each specialist runs concurrently — each on its own dedicated data sources — for comprehensive, fast coverage.

4

Get a Deliverable

Receive a synthesized, cited, and auditable output — not a chat reply. Every finding traces to its source record.

🧭

Co-Pilot Mode

You stay in the loop — review the task manager's plan, add or swap specialists, and steer each step. Best when you want full control over scope and method.

You guide the process
🚀

Autopilot Mode

State the task and the system assembles and runs the entire specialist team automatically, returning the finished deliverable. Best for speed and routine jobs.

Hands-off, end-to-end
Specialists — Pick by Goal

Built for Clinical Research Workflows

Start from your goal and the system proposes the right specialists. Each one is transparent about its research protocol, the data sources it queried, and every finding it cites.

Regulatory Submission

Navigate FDA & Global Pathways

Prepare regulatory strategies, draft submissions, and navigate device and drug pathways with specialists trained on FDA, EMA, and global regulatory frameworks.

FDA Device Regulatory Global Regulatory Pathway Medical Writer Drug Safety Reimbursement Strategy
Evidence & Literature

Know What the Evidence Says

Query PubMed, ClinicalTrials.gov, and clinical databases simultaneously. Receive synthesized, cited literature briefs — GRADE-style summaries and trial landscapes in minutes.

Science Literature Analyst Clinical Evidence Specialist Clinical Trial Analyst Drug Information
Target & Go/No-Go

Assess Targets & Indications

Run structured go/no-go analyses across structure, safety, pathways, indications, and competitive intelligence — backed by validated data, not generative guesses.

Target Assessment Indication Exposure Strategist
IP & Patents

Clear or Protect Intellectual Property

Conduct patent landscape analyses, freedom-to-operate reviews, and drug patent/IP assessments — querying USPTO, EPO, and linked drug databases in parallel.

US Patent Research Analyst Drug Patent/IP
KOLs & Investigators

Find & Rank Experts

Identify and rank key opinion leaders and clinical investigators relevant to your therapeutic area — with sourced publication, trial, and payment-disclosure data.

KOL Scouting Open Payments Data
Launch & Claims

Substantiate Claims & Go to Market

Build PubMed-backed claim dossiers, competitor claim audits, and evidence-backed product content — with regulatory pathway guidance by geography.

Product Science Analyst Claims Verification Marketing Content Regulatory Pathway by Geo
Standing Intelligence

Radar — Always Watching Your Space

"Don't wait for the brief — Radar spots the signal, your task force runs it."

Radar boards join multiple authoritative sources around a question you care about, refresh automatically, and tell you what changed. Any signal can immediately launch a specialist task force for deeper investigation.

Conference ★ Flagship

Medical Conference Tracking

Tracks new abstract titles, readout signals, and citations as they publish — spot competitive moves the moment they surface.

ASCO ASH AACR AHA ADA SABCS
MedTech

Device & Regulatory Intelligence

Monitor device pipelines, CMO activity, and quality signals in real time.

510(k) Pipeline PMA Pipeline De Novo CMO Watch Device Quality
Pharma

Drug & Market Intelligence

Track cliffs, competitive moves, recall risk, and emerging biotech signals.

Patent Cliff Biosimilar Cliff Asset Hunt Emerging Biotech Recall Risk Drug Spend
Supplement

Ingredient & Market Monitoring

Watch ingredient profiles and buyer prospect signals in the supplement and nutraceutical space.

Ingredient Profile Ingredient Buyer Prospects
50+ Authoritative Sources

Grounded in Real Data. Verified to the Source.

Every specialist queries its own dedicated subset of sources — no single query touches all of them. Each result is cited and auditable back to the exact record it came from.

PubMed ClinicalTrials.gov FDA 510(k)/PMA FDA Enforcement Orange/Purple Book openFDA USPTO & EPO Patents CMS Part D Open Payments DailyMed Curated Bioactivity / Knowledge Graph ChEBI PubChem EMA CrossRef + many more

Citation Fidelity Benchmark — Mar 2026 · 180 Queries × 9 Systems × 6 Domains

Generic AI (Gemini 3.0 Pro) — fabricated citations ~29%
Generic AI (GPT-5.5) — fabricated citations ~24%
ResearchNexo IQ — citations verified vs CrossRef/PubMed 95–97%

ResearchNexo IQ only cites sources it actually retrieved, each resolved against CrossRef & PubMed — so fabrication is near-zero, by construction. Verified programmatically, not self-graded.

Real Outputs

Not a Chat Reply — A Business-Ready Deliverable

Every task returns a structured document you can export, share, and act on — with the protocol, data sources, and citations built in.

Biotech & Pharma

Drug & Device Research

  • Investigator's brochures
  • 510(k)/PMA regulatory pathway
  • Patent landscape & FTO
  • IND/NDA support documents
  • KOL maps
  • Trial design & endpoints
Clinical Evidence

Literature & Trial Intelligence

  • Cited literature briefs
  • GRADE-style systematic summaries
  • Clinical Evaluation Reports (CER)
  • Trial landscape analyses
  • Drug information dossiers
Supplement & Nutraceutical

Claims & Formulation

  • PubMed-backed claim dossiers
  • Ingredient safety reviews
  • Claims-to-GTM roadmaps
  • Competitor SKU & claim audits
  • Regulatory pathway by geography
CRO / CDMO / Medical Writing

Site & Operational Intelligence

  • Investigator & site intelligence
  • Recruiting-site landscape
  • Standardized protocol drafting
  • Sourcing & vendor review

Your 650 credits are ready to use.

Log in to Medinexo today and start using your 650 first-month credits — your AI research engine is already included with your membership.

Access ResearchNexo IQ →

ResearchNexo IQ aggregates publicly available, source-attributed data and is not endorsed by or affiliated with NLM, NIH, FDA, USPTO, EMA, or CMS — source data attributed to its owners. Decision-support intelligence, not legal, medical, or investment advice.