
Clinical Trial App Development
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Clinical trials are complex, data-intensive processes that demand accuracy, security, and seamless coordination. Dogtown Media develops custom mobile applications to simplify clinical operations, enable remote patient monitoring, and ensure compliance with industry regulations.
Built for Every Trial Model
From patient recruitment to post-market surveillance, our clinical trial mobile apps support every stage of the development lifecycle—empowering research teams with real-time data, automated workflows, and actionable insights.
We support a variety of medical trials, aligning functionality with regulatory classification and user needs:
- Pharmaceutical Trials: Enable data capture across Phases I–IV, with integrated ePRO tools, appointment scheduling, and adverse event reporting.
- Medical Device Trials: From feasibility to pivotal studies, we build applications that collect performance data and sync with wearable or implantable devices. We also provide support for 510(k) or PMA submissions.
- Novel Therapies: Power gene therapy and personalized medicine trials with apps that accommodate complex patient criteria, custom dashboards, and secure EHR integration.
Core Capabilities

Real-Time
Data Collection
Capture vitals, medication adherence, and symptom progression using mobile sensors and connected devices. Enable proactive interventions through real-time alerts and analytics.

EHR & System
Integration
Ensure seamless interoperability with Electronic Health Records (EHRs) and Clinical Trial Management Systems (CTMS). Our apps integrate via FHIR APIs and HL7 standards to eliminate manual entry and maintain data continuity.

Patient Recruitment & Screening
Digitally streamline participant onboarding with mobile pre-screening, consent workflows, and automated eligibility tracking—reducing time-to-enrollment and improving study diversity.

Appointment & Visit Management
Built-in scheduling tools reduce administrative overhead, enhance protocol adherence, and sync directly to native device calendars with automated push notifications and reminders.

Secure
Communication
In-app messaging and secure patient portals facilitate direct communication between coordinators, investigators, and participants, boosting engagement and reducing dropout rates.

Regulatory
Compliance
All applications are developed with HIPAA, GDPR, and FDA 21 CFR Part 11 compliance in mind. Our solutions include encryption at rest and in transit, role-based access controls, and full audit trails.
Proven Experience in Clinical Trials
Dogtown Media has supported global healthcare organizations in deploying mobile solutions for medical device and pharmaceutical trials:
- Bristol Myers Squibb: Developed a clinical trial app integrating with wearable medical devices to track vitals in real time and issue push alerts for critical thresholds. Included in-app questionnaires to support ePRO data collection.
- National Sleep Foundation (SleepLife®): Created an RPM app connected to Fitbit for sleep tracking, with a physician dashboard and custom survey tools for trial engagement.
- Marathon Health: Delivered a chronic disease management platform for employer-sponsored studies, integrated with Garmin and Fitbit wearables, wellness scores, and appointment tracking.
Focused on Security, Built for Scale
We engineer mobile infrastructure with security-first design:
- End-to-end encryption (AES-256)
- Secure client-server architecture
- Role-based access and identity management
- 2FA and audit logging
- Compliance with HIPAA, GDPR, and 21 CFR Part 11
- Support for 510(k) and PMA documentation workflows
Whether your team is conducting device trials or gene therapy research, we offer mobile solutions that scale with regulatory complexity and clinical need.
Conduct Your Next Clinical Trial With Dogtown Media
Dogtown Media combines deep experience in healthcare mobile app development with a hands-on, collaborative approach. Our team works directly with CROs, sponsors, and research teams to design intuitive, compliant platforms that reduce trial friction and accelerate study completion.
We bring expertise in:
- Medical device application development
- Mobile health UX and accessibility
- Integration of healthcare devices and EHRs
- Remote patient monitoring and wearable syncing
- FDA 510(k) regulatory support
Our mobile apps are not just digital tools—they’re clinical enablers that transform how data is captured, interpreted, and acted upon.