01Interfaces built around real clinical workflows, not assumptions
Shadowed · Ward 4
Chartingback at the stationat the bedside, where nurses are
Physicians spend nearly half their workday in digital systems, and much of that time goes to fighting software. As a healthcare design agency, we build products that work in real clinical settings: fast, clear and designed for HIPAA, FDA and GDPR from the start.
$1 billion+
01Interfaces built around real clinical workflows, not assumptions
Shadowed · Ward 4
Chartingback at the stationat the bedside, where nurses are
02HIPAA, GDPR, FDA and ISO 13485 requirements built into every phase
Compliance · every phase
Complianceone review before launcha piece of every phase
03Tested with clinicians, nurses and patients before launch
Usability test · 3 roles
The lab results screennever tried by its userstried by all three before launch
04Design that prevents errors, not just design that looks clean
Medication search
Picking a drugtwo names that look the samethe difference in capitals
Four clicks to one lab result add up to hours a week. Clinicians feel it as burnout, and teams feel it as turnover.
A mislabeled field sets up a dosing error. Compliance left for after launch means rework and risk.
Clinicians work around tools they don’t trust, and patients drop off portals that confuse them. The budget goes with them.
Research in clinical settings with the people who will use the product: observing real workflows, interviewing clinicians and patients and finding where the current system breaks.
Clean, accessible interfaces for high stress, time pressure and users who can’t stop to read a tooltip. Every visual decision serves workflow speed and error prevention.
EHR UX design that matches how clinicians think and work, cutting documentation burden without losing accuracy. Electronic health records are among the most complex products there are.
Telehealth app design, patient portals, symptom trackers and medication tools for users of every age, digital skill level and health status. Here, accessibility and clarity are the product.
Medical UX design for touchscreen interfaces on diagnostic equipment, infusion pumps and monitors, built to meet FDA human factors requirements and IEC 62366 usability standards.
HIPAA, FDA 21 CFR, ISO 13485 and IEC 62366 treated as design constraints from the first wireframe, including the human factors documentation a submission needs.
MEDORA · MEDICATION ORDER
The system“it passed QA”where it breaks, seen in use
MEDORA · PATIENT CHART
The bannernine fields at one sizewhat matters, at a glance
MEDORA · PROGRESS NOTE · BED 12
Documentationretyping what the chart already knowswriting only what needs a clinician
MEDORA · PATIENT APP · TODAY
Medicinesfine print and a grey linkone dose, one big button
MEDORA · INFUSION PUMP · CHANNEL A
Infusion pumpa tenfold typo runsthe pump stops it first
MEDORA · ORDER CHANGE · 21 CFR PART 11
Audit traila number quietly overwrittenwho, when and why, signed
Healthcare has constraints a general design process doesn’t account for. Ours does.
Time with the people who use the product: workflow observation, structured interviews with clinicians and patients and a review of current pain points. Regulatory requirements get mapped alongside user needs from day one.
DiscoveryAn attending physician, a floor nurse, a patient and a billing administrator can use the same system in completely different ways. Personas and journey maps capture those differences.
PersonasData hierarchy, navigation and workflow logic structured around how clinical decisions get made, not around database schemas or admin convenience.
ArchitectureCritical clinical flows are wireframed before visual design. Prototypes are tested in conditions close to clinical reality, with time pressure and interruptions included.
PrototypesStructured sessions with clinicians, nurses and patients from your user base, with close attention to error recovery: what happens when something goes wrong, and whether users recover without risk to the patient.
TestingDev-ready specs, an annotated component library and the design documentation regulators ask for: human factors reports, use error risk analysis and formative usability findings where FDA or other agencies require them.
HandoffResearch happens on the ward and in the clinic, with the people who will use the product.
A clinician with 20 patients and no time, a patient of 80. If it works for them, it works for everyone.
HIPAA, FDA, GDPR and ISO 13485 shape the design, with the documents a submission needs.
Research to handoff with one team. Every file, library and document is yours.

“About a week ago, we went a bit viral with 10k users in 2 days and we received a lot of positive feedback about the design - so thank you Glow for that!”
Israel Benarousse·CEO, Dropcall
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“Glow Design Agency delivered high-quality UX/UI designs that enabled the client to close more deals. Their animated video and design gained the client almost 500+ new LinkedIn followers. The team executed work on time and within budget.
Doug Marinaro·CEO, Riptide

"The design work provided by Glow Design Agency completely exceeded project stakeholder expectations in terms of both quality and delivery. Their team was organized and communicative throughout the process, breaking down complex industry concepts and translating them into a sleek and useable UI."
Jon Fry·CEO & Founder at Lendflow (YC W21)
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"Glow Design provided UI/UX design for a office space provider and has since expanded their role to include design updates for the site's front- and backend as well as social media visuals and animations."
Eric Zellhart·VP Product at LiquidSpace
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"Glow Design Agency provided UI and UX design services for e-cars charging market company. They were tasked with designing the UX and UI of the app's prototype."
Max Grollmann·Managing Director
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"Glow was hired by an e-commerce platform for their UI/UX design services. They redesigned website and provided support. After the new website was launched, the client saw a significant increase in conversions."
Vinicius Rodrigues·CTO at E-Commerce Platform
Registering one patient took 8 to 10 minutes across five systems with duplicate data entry. One unified workflow cut it to 3 minutes and saved staff about 30 minutes a day.
Long registration and multi-screen intake forms kept patients from their first consultation. One-tap consultation start, minimal required fields and clear navigation turned that around in year one.
Physicians spent 40% of documentation time navigating instead of entering data. An information architecture restructure and contextual navigation cut that time and improved documentation completion.
Healthcare UX design is the practice of designing clinical and patient-facing software so it’s safe, fast and easy to use under real conditions: time pressure, interruptions, mixed digital skills and strict regulation. The goal is fewer errors, faster workflows and products clinicians and patients actually adopt.
Healthcare UX design is the practice of designing clinical and patient-facing software so it’s safe, fast and easy to use under real conditions: time pressure, interruptions, mixed digital skills and strict regulation. The goal is fewer errors, faster workflows and products clinicians and patients actually adopt.
It depends on scope. A focused usability study and redesign of one clinical workflow can take 4 to 6 weeks. A full engagement with research, UX strategy, UI, prototyping, testing and compliance documentation usually runs 3 to 5 months. You get a realistic timeline before work starts.
It depends on scope. A focused usability study and redesign of one clinical workflow can take 4 to 6 weeks. A full engagement with research, UX strategy, UI, prototyping, testing and compliance documentation usually runs 3 to 5 months. You get a realistic timeline before work starts.
Yes, a good share of our healthcare work is with startups building their first clinical product. We shape the engagement around your stage, starting with the highest-risk design decisions and building out as the product and funding grow.
Yes, a good share of our healthcare work is with startups building their first clinical product. We shape the engagement around your stage, starting with the highest-risk design decisions and building out as the product and funding grow.
Yes. We usually start with a UX audit of the live product, find where users struggle most and build the redesign on that evidence. For regulated products, we also review existing usability documentation before proposing changes.
Yes. We usually start with a UX audit of the live product, find where users struggle most and build the redesign on that evidence. For regulated products, we also review existing usability documentation before proposing changes.
We treat HIPAA, FDA 21 CFR requirements, ISO 13485 and IEC 62366 as design constraints from the start. That means data access patterns that support audit logging, authentication UX that meets security requirements and the human factors documentation FDA submissions require. Your regulatory team is involved throughout, not only at handoff.
We treat HIPAA, FDA 21 CFR requirements, ISO 13485 and IEC 62366 as design constraints from the start. That means data access patterns that support audit logging, authentication UX that meets security requirements and the human factors documentation FDA submissions require. Your regulatory team is involved throughout, not only at handoff.
It depends on the number of user types, the complexity of clinical workflows, the regulatory requirements and how much usability testing you need. Fixing a design problem in a live clinical system, especially a regulated one, costs far more than fixing it during design. We’ll give you a realistic estimate after a first call.
It depends on the number of user types, the complexity of clinical workflows, the regulatory requirements and how much usability testing you need. Fixing a design problem in a live clinical system, especially a regulated one, costs far more than fixing it during design. We’ll give you a realistic estimate after a first call.
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