← All Services
Service 04 · Future Trity Pharma

Wearable Skin Devices

Dermal sensors for continuous, clinical-grade monitoring.

5.8dAverage Wear Time
97%Reference Agreement
HIPAAData Compliance
Why this matters

Built around the business reality of your team.

The next decade of medicine is continuous, not episodic. Chronic disease, decentralised trials, and home-based care all depend on devices that patients will actually wear — and data that clinicians can actually trust. Future Trity's dermal sensor platform was built for both audiences.

Most wearables are wellness toys with clinical aspirations. We build the inverse: medical-grade devices engineered to ISO 13485 with consumer-grade comfort and adherence.

Our approach

A method, not just a capability.

01

Skin-conformal electronics with multi-day wear comfort.

02

Edge analytics that preserve battery and protect patient data.

03

Validated against gold-standard clinical reference devices.

04

Open APIs for integration with EHRs and trial platforms.

What you receive

Clear deliverables, audit-ready documentation.

Continuous Vital Signs

Heart rate, respiration, temperature, hydration, and SpO2 from a single patch.

Biochemical Sensing

Glucose, lactate, and electrolyte monitoring via interstitial fluid.

Decentralised Trial Kits

Patient onboarding, data capture, and adherence tooling for remote studies.

Custom Sensor Development

Co-engineered devices for proprietary endpoints and biomarkers.

Why we're the right partner

The difference is in the discipline.

01

ISO 13485 Certified

Full medical device quality system, not a consumer-electronics shortcut.

02

Clinical Validation

Published agreement studies vs. reference standards across major endpoints.

03

Adherence-First Design

Average 5.8 day wear time — patients actually keep them on.

04

Integrated Data Platform

HIPAA and GDPR-compliant cloud with clinician dashboards out of the box.

Start the conversation

Building a decentralised trial, chronic care program, or new clinical endpoint?

Our team responds within one business day with a tailored capability brief and next-step proposal.

Request a Quote · 04

Brief our Wearable Skin Devices team.

Submissions are reviewed by the capability lead within one business day. All information is treated as confidential under our standard Mutual NDA framework.

01

Capability lead acknowledges within 24 business hours with a reference number.

02

Mutual NDA executed prior to detailed technical exchange.

03

Scoping call with subject-matter experts and a written capability brief.

Adverse event reportingThis form is not a channel for reporting adverse events, product quality complaints, or medical information requests. Contact pv@futuretreaty.com for pharmacovigilance matters.
!
Regulatory & Compliance Notice

By submitting this request, you confirm that the information provided is accurate and relates to a legitimate business inquiry. Do not include patient-identifiable data, proprietary third-party information, or any material restricted under export-control regulations (EAR, ITAR, EU Dual-Use). Future Trity Pharma Ltd. operates under EU GMP, FDA 21 CFR Part 210/211, WHO GDP, ISO 9001:2015 and ISO 13485 quality systems. Any subsequent engagement is subject to Mutual NDA, anti-bribery (UKBA / FCPA), and modern slavery (UK MSA 2015) compliance review.

Transmitted over TLS · Stored under ISO 27001 controls · Retained for 24 months.