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AR and VR content for medical training and education

Medical AR/VR & Immersive Media

Pubrica develops medical AR/VR and immersive media for medical device companies, surgical training programs and teaching hospitals, patient education teams, medical affairs and marketing teams, and rehabilitation programs. Each project delivers an immersive experience build (AR app, VR module or web-based 3D experience), 3D anatomy, procedure or device models, interaction design for the target platform, a deployment package for the target hardware and a content update plan, developed with reference to FDA guidance on software/AR-VR as medical devices. Our medical illustrators, 3D animators and UX/UI designers work in-house. A named subject specialist manages your project from brief to delivery, and a second, independent reviewer checks the work before it reaches you.

  • Immersive experience build — included in every engagement
  • 3D anatomy/procedure/device models built to the required fidelity — included in every engagement
  • Interaction design and user flow for the target device/platform — included in every engagement
  • Produced to named standards, including FDA guidance on software/AR-VR as medical devices
  • Scoped pricing: a quote provided after a short scoping call
What is included What is not included

Immersive experience buildIncluded

3D anatomy/procedure/device models built to the required fidelityIncluded

Interaction design and user flow for the target device/platformIncluded

Deployment package for the target hardwareIncluded

A flat price with no scoping callNot included

Brief → scoping → draft → delivered

Every engagement
  • Immersive experience build
  • 3D anatomy/procedure/device models built to the required fidelity
  • Interaction design and user flow for the target device/platform
  • Deployment package for the target hardware
  • Content update plan for post-launch revisions
Scoped quoteQuoted after a short scoping call
10–15 business daysFrom brief to final delivery
5 deliverablesListed in full below
ISO 9001:2015Quality management certified · cert. H3CR9TCU20251212INDQM10N

Deliverables

Five Core Medical AR/VR Deliverables

Every item below is produced in-house by Pubrica’s medical illustrators, 3D animators and UX/UI designers and checked by a second, independent reviewer before delivery.

Immersive experience build Immersive experience build (AR app, VR module, or web-based 3D experience).
3D anatomy/procedure/device models built to the required fidelity 3D anatomy/procedure/device models built to the required fidelity.
Interaction design and user flow for the target device/platform Interaction design and user flow for the target device/platform.
Deployment package for the target hardware Deployment package for the target hardware (headset, tablet, kiosk).
Content update plan for post-launch revisions Content update plan for post-launch revisions.

Who We Serve

Five Client Groups We Support with Medical AR/VR

The organizations below commission this service, and each project is planned around the audience who will use the material.

Medical device companies demoing products at congresses and trade showsA client group that commissions this service directly.
Surgical training programs and teaching hospitalsBuilding simulation modules
Patient education teams explaining procedures or anatomy to patients and familiesA client group that commissions this service directly.
Medical affairs/marketing teams wanting a memorable interactive booth experienceA client group that commissions this service directly.
Rehabilitation and physical therapy programsBuilding interactive exercise tools

Compliance and Standards

Medical AR/VR Standards and Guidelines

The regulatory codes, guidelines and quality standards that apply to this service.

FDAARVR

FDA guidance on software/AR-VR as medical devices

AR/VR tools used for surgical navigation or diagnostic overlay can qualify as medical device software subject to FDA review, depending on intended use.

HIPAA

HIPAA

Patient-specific anatomy models or tele-consultation features built on patient imaging data must be designed around HIPAA data handling and privacy requirements.

W22W

WCAG 2.2 (where applicable to companion interfaces)

Any 2D companion UI (menus, controls) built alongside an immersive experience should meet accessibility standards for users with disabilities.

ISO9001:2015

Quality management (cert. H3CR9TCU20251212INDQM10N)

Governs how each project is managed, reviewed and documented.

Responsible Use of AI

Our Approach to AI Use in Medical AR/VR

Generative tools are useful for drafting and iteration. They are not used anywhere the output could be mistaken for verified clinical data or a real patient.

What we use it forLayout variations, colour systems, and first-pass drafts that a human then corrects against the brief and the brand or clinical standards that apply.
What we do not use it forGenerating any image, figure or quote presented as real clinical data, a real patient, or a verified result; and nothing goes out without a named reviewer's sign-off.
What we include in your AI declarationThe tool, the stage it was used at, and the human oversight applied — because MLR/PRC reviewers, funders and regulators increasingly expect this stated rather than assumed.

Why we do not publish AI accuracy figures

Accuracy figures for AI design and content tools are usually reported by the vendors that sell them.

For this reason we do not quote an accuracy figure of our own. We tell you which tool was used on your project, at which stage, and what a named reviewer changed afterwards.

Our Process

Medical AR/VR Process: Four Steps with Draft Review

Each project moves from brief and scoping to a reviewed first draft, then to revisions and final delivery.

Step one

Submit Your Brief and Reference Material

Send us what the experience needs to communicate, who will see it and anything that must or must not appear, together with any existing assets, brand guidelines or source material we should work from.

Step two

Initial Scoping Discussion

We confirm the audience, the applicable standards and, for scoped work, the factors that determine the final price, so the quote is agreed before work begins.

Step three

Concept and First Draft

A subject specialist and the production team build the first version against the brief, reviewed internally for accuracy before it reaches you.

Step four

Revisions and Final Delivery

We incorporate your revisions and deliver the files listed on this page, including the working files, so the material can be updated later without starting again.

Request a Free Scoping Assessment for Your Medical AR/VR Project

We confirm the cost, timeline and applicable standards before you commit to anything. The assessment is free and is completed within two business days.

What you provide
The briefThe purpose of the material and its intended audience
Reference materialExisting assets, brand or style guidelines, prior approved versions
The audienceClinician, patient, payer, investor or internal team
ConstraintsAnything that must or must not appear, and the standards that apply
The deadlineYour deadline, including any congress or submission window
Approval routeWho approves the work, and whether MLR/PRC review is part of the process

Our Experts

Your Medical AR/VR Team

The same named team of specialists stays with your project from scoping to delivery.

Subject expertSubject matter expert matched to your topic

Determines which claims the evidence supports. The subject expert is matched to your topic and tells you clearly when the brief asks for something the evidence does not support.

OwnsScope, judgement, interpretation
Reviews againstThe applicable standards for this work
FieldMatched to your topic
Dr. DivyaPhD in Life Science · second reviewer

Reviews the work independently of the first pass and reconciles the two, because most errors in this work are factual rather than errors of reasoning. Disagreements are logged and adjudicated.

OwnsIndependent second read
Reviews againstThe applicable checklist
Adjudicated byA third reviewer
Dr. AntonyProduction and delivery lead

Responsible for file formats, compliance with the destination specification and the handover of working files, so that the delivered files match what you requested.

OwnsProduction and delivery
Reviews againstThe destination's own specification
Second-checked byA second production reviewer
Mr. JohnCompliance and standards reviewer

Confirms that the work meets the standards that apply to it, whether MLR, WCAG, a regulatory guidance or the body that governs the specific deliverable.

OwnsStandards and compliance review
Reviews againstThe standards listed on this page
ToolsThe current published guidance for each

Evidence Base

The Evidence and Expertise Behind Our Medical AR/VR Services

Each point below is sourced from published research or guidance, or owned by a named role on the team. We can direct you to the source or the reviewer on request.

01 VR simulation is now a credible training formatPublished comparisons of VR surgical simulation with physical simulation have found comparable trainee performance, which is why VR is now treated as a credible training format rather than a novelty.
02 Trainee utility ratings by training formatIn the same 2022 randomized study of 21 orthopaedic trainees (Margalit et al., JAAOS Global Research and Reviews), utility ratings differed significantly across groups (p=0.001): physical simulation 10 out of 10, VR 7, and reading and video 6.
03 Claims agreed by a named subject specialistA named subject specialist, matched to your topic, decides which claims the immersive experience may make before any drafting begins.
04 Independent second review before deliveryA second, independent reviewer checks the immersive experience build before it reaches you, and any disagreements between reviewers are formally adjudicated.
05 Developed with reference to FDA guidanceWork is developed against FDA guidance on software/AR-VR as medical devices, which is named on this page.
06 Working files handed over on deliveryWorking files are handed over on delivery, so the material can be updated later without starting again or paying for the work twice.

Packages

Medical AR/VR Pricing Based on Project Scope

This service is priced after a short scoping call, because the cost depends on the project factors listed below.

Scoped

Medical AR/VR & Immersive Media

The final price is set by the project factors listed below.

Scoped quoteAfter a short, free scoping call

Delivery Set at scoping, typically 10–15 business days

  • ✓Use case (surgical training simulation vs. patient education vs. congress/trade-show demo)
  • ✓Platform target (standalone VR headset, AR mobile/tablet, web-based 3D, or multi-platform)
  • ✓Content complexity (number and fidelity of 3D anatomy/procedure models, interactivity, haptic feedback)
  • ✓Integration needs (patient imaging data, EHR, or device data feeding a personalized model)
  • ✓Deployment and support scope (number of install sites/events, ongoing content updates)
Get a scoped quote

Quality Assurance

Our Service Commitment and Revision Policy

The revision commitment that applies to every project, with its scope and remedy stated in advance.

The Pubrica revision commitment

Free Revision Where Work Does Not Meet the Agreed Brief or Named Standard

Within the agreed scope, we revise at no extra cost any work that does not match the brief or a standard named on this page.

01

The brief is confirmed before production

Confirming the brief at scoping prevents misunderstandings that would otherwise require rework after delivery.

02

A named reviewer signs off before you see it

The review is made against the standards listed on this page.

03

AI use is disclosed

We tell you which tool was used, at which stage, and what a human reviewer changed afterwards.

04

You receive the working files

The material can be updated later without starting again or paying for the work twice.

Client Stories

“The illustration was scientifically accurate and the revisions were fast. It went into the deck without a single correction from medical affairs.”
Dr. KatherineMarketing lead, medical device company

USA

FAQs

Frequently Asked Questions About Medical AR/VR

If your question is not answered here, ask an expert — no quote required.

Pubrica develops medical AR/VR and immersive media for medical device companies, surgical training programs and teaching hospitals, patient education teams, medical affairs and marketing teams, and rehabilitation programs. Each project delivers an immersive experience build (AR app, VR module or web-based 3D experience), 3D anatomy, procedure or device models, interaction design for the target platform, a deployment package for the target hardware and a content update plan, developed with reference to FDA guidance on software/AR-VR as medical devices. Our medical illustrators, 3D animators and UX/UI designers work in-house. A named subject specialist manages your project from brief to delivery, and a second, independent reviewer checks the work before it reaches you.

The core deliverable is an immersive experience build (AR app, VR module, or web-based 3D experience); the full list appears under “Deliverables” on this page.

Published comparisons of VR surgical simulation with physical simulation have found comparable trainee performance, which is why VR is now treated as a credible training format rather than a novelty.

This requirement is documented in published research and regulatory guidance, so our specialists address it as a defined part of every project.

The cost depends on several project-specific factors: Use case (surgical training simulation vs. patient education vs. congress/trade-show demo); Platform target (standalone VR headset, AR mobile/tablet, web-based 3D, or multi-platform); Content complexity (number and fidelity of 3D anatomy/procedure models, interactivity, haptic feedback); Integration needs (patient imaging data, EHR, or device data feeding a personalized model).

A single flat price would not reflect these differences, so we agree the price in a short scoping call before you commit to anything.

Medical device companies demoing products at congresses and trade shows

Surgical training programs and teaching hospitals commission it to build simulation modules.

AR/VR tools used for surgical navigation or diagnostic overlay can qualify as medical device software subject to FDA review, depending on intended use.

We apply this standard from the start of each project rather than correcting for it after a reviewer raises it.

Request a Free Medical AR/VR Scoping Assessment

Receive a free assessment of cost, timeline and applicable standards within two business days.

Get a free quote

Regulations

Check your project against this rule

  1. 1Your work
  2. 2Your details
  3. 3Send
What do you need?

Material you send is held under signed confidentiality, with access limited to the assigned team and encrypted transfer. It is not used to train anything and is not passed to third-party tools. Ask for the agreement before you send anything you would rather cover first.