A clinical operating system

Cell therapy,
structured as software.

Seven capsules — patient selection, training, regulation, decision support, and a working developer engine — built around stromal vascular fraction. Bilingual. Bedside-ready. Built for the partners who ship cell therapy at scale.

00
Clinical capsules
00
Modules total
2·5
Free / Paid capsules
The pipeline

From tissue to registry,
in five disciplined moves.

/ 01 Collect Lipoaspirate / 02 Process Minimal manipulation / 03 Deliver Image-guided / 04 Monitor PROMs · safety / 05 Register Outcome registry
Each stage maps to a capsule. The platform owns the full tissue-to-data loop.
Access

Two capsules free.
Five behind a clinical license.

The full clinical bundle

The complete platform — six clinical-license capsules plus the master overview — delivered as a single self-contained download. Use it inside your clinic, your training programme, or your next trial. Built for partners who ship cell therapy at scale.

  • Knee · osteoarthritis pathway
  • Spine · discogenic & facet logic
  • Sports & soft tissue · tendon, muscle, repair
  • Business & regulatory · model, cost, risk
  • Developer · clinical engine + registry schema
  • Master overview · the single-file application
$4,900
USD · single-clinic license
Unlock the bundle
Settled in ETH / USDC / USDT (ERC-20)
The platform

Seven capsules. One clinical platform.

The biology

One tissue. Four lineages. Three regenerative effects.

/ SOURCE Adipose tissue Lipoaspirate · minimally manipulated centrifugation / STROMAL VASCULAR FRACTION ASC EPC PCT MAC Heterogeneous cell pool ASC · EPC · pericyte · macrophage paracrine + cellular / EFFECT Angiogenesis Anti-inflammatory Trophic regeneration Tissue niche reset
Source → cells → effects · the platform owns each surface
Why it exists

Cell therapy is sold as a kit.
It should ship as a system.

A kit alone teaches no one. The clinic that buys it inherits a hundred unanswered questions — which patients qualify, which contraindications are absolute, what the consent must include, how follow-up is captured, what the registry looks like, what the regulator allows.

The SVF Clinical Platform is the layer that sits between the kit and the patient. Seven capsules, one shared logic, and a working developer engine for anyone who wants to turn cell biology into software.

For device manufacturers
Ships as the training and decision-support layer bundled with every kit. Clinics activate faster. Sales stick longer.
For clinic networks
Standardised patient selection across sites. OSCE-based investigator certification. A registry schema that produces publishable data.
For trial sponsors
The protocol skeleton, registry schema, safety frame, and analytic plan in one ready-to-customise system.
The foundation

A platform built on the evidence,
not on opinion.

Clinical foundation
Three major systematic reviews and over one hundred primary citations across orthopaedic and regenerative literature.
Modular architecture
Seven independent capsules sharing one clinical logic, one safety frame, one registry vocabulary.
Deployment ready
Browser-based, hostable on any infrastructure, white-label ready for partner branding.

The platform synthesises the major systematic reviews on adipose-derived therapies — Lana 2022, Goncharov 2023, Hohmann 2025 — and the most recent literature on niche reconstruction in bone, cartilage, and soft-tissue regeneration.

Each capsule is engineered as an independent surface, yet all seven share one common clinical logic — the same patient-selection grammar, the same safety frame, the same registry vocabulary. The result is a platform that a partner can adopt whole, fork into a private edition, or absorb into an existing product line under their own brand.

Built by a clinical regenerative medicine team across a year of reading, modelling, and capsule iteration — designed for the partners who ship cell therapy at scale.

Version 1.0 — A clinical layer for cell therapy
Regulatory notice Educational and clinical-decision-support content. Not approved by FDA, EMA, or any regulatory agency as a medical device, and not a substitute for clinician judgement, institutional review, or applicable regulatory authorisation in your jurisdiction. Stromal vascular fraction therapy is positioned and used differently across regulatory regimes — verify local rules before any clinical application. Use only by licensed clinicians within the legal framework of the site of care.

A clinical layer is missing from cell therapy.
This is it.

Two capsules free in your browser. Unlock the full clinical bundle for a single-clinic license.

Unlock the clinical bundle