About MedGrid

We built MedGrid to answer the one question medicine has always dodged.

"How do we know if something actually works?"

For a hundred years, medicine has run on anecdote, authority, and assumption. We're replacing that with a verified data layer — connecting molecule to protocol to patient to outcome, in one platform.

01 / Origin

It started inside a clinic, not a boardroom.

Medicine ships products. The reps close. The doctors prescribe. The patients improve. And then — the same thing happens everywhere — the outcome disappears. No structured record, no attribution, no proof.

The industry has a sales engine. It has never had a data engine. So we built one.

MedGrid is what happens when the people who actually move the product decide to keep score.

Every product transacted on MedGrid is auto-linked to the patient record at the moment of purchase. The outcome no longer disappears — it becomes the asset.

02 / Platform

A clinical intelligence engine, shipped in layers.

MedGrid is the connective tissue across five things that should already be connected. We're shipping it one layer at a time — openly. Layer 1 is live today.

01
Order
ERP · Marketplace

Every product transacted on MedGrid is auto-linked to the patient record at the moment of purchase. The catalog is live, with verified vendors onboarding into every specialty.

Live today
02
Protocol
Med Director · Compliance

Med Director–approved protocol library, plus physician-authored custom protocols inside our compliance framework. Ships in the next release.

In pipeline
03
Outcome
ClinicalX Engine

Structured 30 / 60 / 90 day capture — labs, PROs, physician assessment. The asset that proves what works. Targeting Q3 2026.

Coming soon
04
Intelligence
Genesis AI · 37M+ articles

Self-hosted GPU infrastructure with 37M+ PubMed articles already indexed. The 10-agent suite rolls out in alpha; outcomes-grounded retraining begins as data accrues.

In pipeline
05
Publishing
Forum · Knowledge Base

Case-study publishing, peer review, KOL reputation engine. Phase 2 — the layer that turns captured outcomes into published evidence.

Coming soon
03 / Compounding

Every participant makes the platform more valuable for every other.

Every physician that joins, every product ordered, every outcome captured makes the protocols better — which attracts more physicians. The longer MedGrid runs, the better the data, the better the AI, the better the outcomes.

This is compounding infrastructure, not software.

04 / By the numbers

The math of compounding evidence.

10,000+
Doctors served via Skydell Medical
69+
SKUs in the launch catalog
37M+
PubMed articles indexed in Genesis AI
10
Specialized AI agents in the suite
5
Platform layers shipping in releases
NPI
Verified access only
Forward-looking targets are projections, not guarantees.
05 / The MedGrid Standard

Held to a standard of care.

Every vendor, every product, every protocol on MedGrid is evaluated across three pillars — the framework for medical infrastructure built around what's best for patients.

01

Regulatory Compliance

FDA-registered manufacturing, cGMP / cGTP, 21 CFR Part 1271, USP <71> / <85>, and 503A & 503B verification. Vendors don't list until diligence clears.

  • FDA registration verified
  • cGMP / cGTP manufacturing
  • 503A · 503B compliant
  • USP sterility & endotoxin
02

Scientific Integrity

Protocols grounded in peer-reviewed evidence and structured outcome capture. What's on MedGrid is what the literature supports.

  • Peer-reviewed protocol library
  • Structured 30 / 60 / 90 outcomes
  • Genesis AI · 37M+ articles indexed
  • COA & batch traceability
03

Clinical Application

Practitioner-tested in real clinical settings. Products are rated on Safety, Efficacy, and Ease of Use by the doctors who use them — not the manufacturer.

  • Safety rating — doctor-verified
  • Efficacy rating — peer-verified
  • Ease of Use rating — practitioner-verified
  • Customer service rating per vendor
06 / Trust & Compliance

Built to hold a regulated industry.

HIPAA-aligned today. Genesis AI runs on self-hosted GPU clusters — no patient data ever leaves our infrastructure, and we never expose patient data to OpenAI, Google, or Microsoft.

U.S. Federal

HIPAA, FDCA §503A/§503B, the Controlled Substances Act, the Ryan Haight Act, FDA device rules, FTC §5.

State-by-State

Medical, pharmacy, and telehealth board rules; state controlled-substance schedules; CPRA, CDPA, CPA, CTDPA, UCPA, MHMD privacy laws.

International

GDPR / UK GDPR, PIPEDA, Quebec Law 25, LGPD, Australia Privacy Act, FADP, plus local prescribing/import rules wherever a user sits.

HIPAA-aligned GDPR-aligned State Med-Board Verified NPI & DEA Credentialed SOC 2 Type II — in progress LegitScript — in progress ISO 27001 — Phase 2

State law often imposes stricter obligations than federal law, and some features are simply not lawful in every state or country. We track this on the State & Country Availability Matrix — and the platform automatically blocks a feature for accounts in jurisdictions where it is not lawful.

Join MedGrid

Stop guessing. Start proving.

Join the physicians, clinics, and manufacturers building MedGrid release by release.

Apply Free — Independent Physician Talk to us