15+
Years of Experience
Pharma App Development Company
AI-first engineering for pharma: adherence modelling and real-world-evidence analytics inside validation-ready processes, clinical trial platforms, patient adherence apps, cold chain monitoring and pharmacy commerce that meet HIPAA, GxP and 21 CFR Part 11 expectations.
- 2010
- Operating since
- 9,000+
- Projects delivered
- 3,900+
- Apps published
- 120+
- AI products shipped
Trusted by the brands we build for
55+
Life-Sciences Projects Delivered
200K+
Trial Participants Supported
HIPAA
& GxP Compliant Builds
Pharma solutions engineered for compliance
From the lab bench to the pharmacy shelf, we digitize the entire chain of care.
Clinical trial platforms
ePRO/eCOA capture, site management, and participant engagement for trials. Clean source data at the point of capture means fewer queries and faster database lock.
- ✓ePRO/eCOA Capture
- ✓Site Management Workflows
- ✓Adverse Event Reporting
- ✓Subject Enrollment & Visit Tracking
Patient adherence apps
Dosing reminders, refill tracking, and outcomes data that clinicians trust. Better adherence data supports the real-world evidence story your medical team needs.
- ✓Dosing & Refill Reminders
- ✓Symptom & Outcome Logging
- ✓Consent-Based Data Sharing
- ✓Offline Capture for Low Connectivity
Drug information portals
Physician reference content, interaction checks, and sample request flows. Field teams get accurate, version-controlled content instead of emailed PDFs of uncertain vintage.
- ✓Version-Controlled Content Delivery
- ✓Interaction Check APIs
- ✓Sample Request Workflows
- ✓Field-Team Content Analytics
Cold chain monitoring
Temperature telemetry and excursion alerts for vaccines and biologics. Every excursion is captured, attributed, and reportable, before the product reaches a patient.
- ✓Temperature Telemetry Ingestion
- ✓Excursion Alerting & Attribution
- ✓Chain-of-Custody Records
- ✓Regulatory Excursion Reports
Pharmacy E-commerce
Prescription upload, verification workflows, and doorstep delivery. Compliance checkpoints sit inside the purchase flow, not bolted on beside it.
- ✓Prescription Upload & Verification
- ✓Compliance Checkpoints in Checkout
- ✓Order & Delivery Tracking
- ✓Patient Identity Verification
Regulatory & quality systems
Document control, audit trails, and validated change management. Your QA team gets the electronic records Part 11 expects, generated by the system rather than reconstructed after the fact.
- ✓Audit Trails & Electronic Signatures
- ✓Document Control (SOPs, Protocols)
- ✓Data Integrity Monitoring
- ✓Submission-Ready Exports
A complete pharma stack across every role
Patients, sites, and quality teams, each with validated, purpose-built tools.
Patient / participant app
Built for trust, privacy, and daily use. Retention in a trial is a clinical outcome, so we design adherence tooling that people actually keep using for the full protocol.
- ✓ePRO Questionnaire Capture
- ✓Dosing & Refill Reminders
- ✓Symptom & Outcome Logging
- ✓Secure Health Data Sharing
- ✓Offline Mode for Low Connectivity
Site & clinician portal
Trial operations without the paperwork pile. Coordinators spend their hours on patients instead of transcription, and sponsors get cleaner data per visit.
- ✓Subject Enrollment & Screening
- ✓eCOA Data Entry
- ✓Visit Scheduling & Tracking
- ✓Adverse Event Reporting
Quality & admin console
The compliance backbone of your program. Audit trails, document control, and data-integrity checks are the product here, not features retrofitted for an inspection.
- ✓Audit Trail & Electronic Signatures
- ✓Document Control (SOPs, Protocols)
- ✓Data Integrity Monitoring
- ✓Regulatory Submission Exports
Life-sciences projects that withstood scrutiny
Heineken
Nutrition and wellness research platform collecting consumer health survey data at scale.
300K+
Survey Responses
100%
Data Integrity Checks
40%
Faster Analysis
Marvel Studios
Fan wellness challenge app with health tracking, gamification, and privacy controls.
750K+
Active Participants
62%
Weekly Retention
4.7★
App Rating
/05
Why choose Moxace for pharma app development
We speak both engineering and regulatory, so your app passes review the first time.
Validation-ready delivery
IQ/OQ/PQ documentation, UAT scripts, and traceability matrices included. Validation is scheduled into delivery, not discovered as a gap after go-live.
Health-data security by default
HIPAA-grade encryption, BAA-friendly architecture, and full audit trails. Security review is a checklist on every release, which is the only version of 'secure' that survives an audit.
GxP process discipline
Change control, configuration management, and 21 CFR Part 11 e-signature support. When your validated system changes, the change itself is documented, automatically.
Clinical domain depth
We've built for CROs, sponsors, and device makers across Phase I-IV programs. You explain the protocol once; we already know what ePRO means.
Participant-centered design
Accessibility-first UX that keeps trial completion rates high. Every percentage point of retention is statistical power you don't have to buy back with enrollment.
Delivery discipline that survives validation
Fixed-price increments with validation testing scheduled in from day one, plus 60 days of post-launch support and 12 months of updates on every build. You receive 100% of the source code, so the system outlives any single vendor relationship.
How a Life-sciences build runs with Moxace
Validation is a scheduled phase, never a discovered gap.
- 01
Discovery & protocol mapping
We map the protocol, workflow and regulatory scope first, and hand your quality team the validation strategy with the quote.
✓ step 01 complete - 02
Architecture & data integrity
Audit trails, e-signatures and 21 CFR Part 11 controls designed into the data model, not retrofitted.
✓ step 02 complete - 03
Agile build sprints
Two-week sprints with traceability maintained as code is written, so the matrix is never a scramble.
✓ step 03 complete - 04
IQ/OQ/PQ & UAT
Installation, operational and performance qualification executed against scripted tests with your QA team.
✓ step 04 complete - 05
Launch & support
Controlled rollout with 60 days of dedicated post-launch support, 12 months of updates and change control thereafter.
✓ step 05 complete
The stack behind our pharma platforms
Compliance-grade engineering from ePRO to cold chain.
Mobile & ePRO
Swift, Kotlin and Flutter apps with offline questionnaire capture and encryption at rest.
Interoperability
HL7, FHIR and REST integrations with Epic, Cerner, Medidata and Veeva.
Cold chain IoT
Temperature telemetry ingestion with excursion alerting and attribution.
AI & Real-world evidence
Adherence modelling and outcome analytics from our AI development services practice.
Patient commerce
Pharmacy e-commerce built on our healthcare app development patterns, with prescription verification inside the purchase flow.
Cloud & devOps
HIPAA-aligned AWS and Azure deployments with BAA-friendly architecture and change control.
FAQ's
$ moxace launch --nowReady to build software that passes audit?
Get a free compliance architecture review and validation plan from our life-sciences team.
- 01
Share your idea
a quick call, no deck required
- 02
See the live demo
every screen, admin to user
- 03
Launch with source
full code, your brand, your servers
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