Clinical Research Software Development

Custom Clinical Research Software, Built for Precision and Compliance

From EDC to CTMS, we design and develop secure, compliant software tailored to your study protocols—so you can accelerate trials, ensure data integrity, and stay audit-ready.

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Why Top CROs and Research Teams Choose Us

Clinical-Grade Expertise

105+ projects delivered across 14 countries—trusted by leading CROs, research orgs, and pharma brands.

End-to-End Compliance

Built to meet HIPAA, GDPR, 21 CFR Part 11, HL7/FHIR, and ABHA standards from day one.

Plug-and-Play Integrations

Seamless connectivity with EHRs, EDC systems, CRMs, wearable APIs, and real-time analytics tools.

MVPs in 4 to 8 Weeks

Build faster without compromising on quality—with PMs and tech leads guiding every sprint.

Full Lifecycle Support

From static MVPs to live deployments, validation testing, and ongoing maintenance.

Flexible Pricing Models

Hourly pricing Or scope-based pricing—depending on what best suits your project’s size, complexity and timeline.

Client Success Stories in Clinical Research

Formly (Tata Memorial): Oncology Disease Registry Platform

Built a clinical data platform for oncologists to manage and analyze cancer registries. ✅ Boosted data quality and collection speed ✅ Empowered clinicians with instant patient insights

Tailored Solutions for Clinical Research Software

Clinical Trials Management Software (CTMS)

Track site performance, enrollment, and trial progress in one place.

Electronic Data Capture (EDC)

Real-time data collection with built-in audit trails and regulatory workflows.

Remote Patient Monitoring (RPM)

Integrate wearables and mobile sensors for continuous vitals tracking.

Health Data Collection Platforms

Scalable platforms to manage high-volume clinical data sets.

Disease Registry Systems

Custom registry tools with longitudinal patient tracking and analytics.

Non-Invasive Diagnostic Tools

Build platforms for remote, device-based diagnostic testing and reporting.

Our Process: From Idea to Industry-Ready Platform

Let's Talk About Your Use Case

Discovery & Requirements Mapping

Deep dive into your protocols, user flows, and compliance needs.

UX/UI Design

Researcher- and participant-focused interfaces to maximize usability.

Agile Development

Sprint-based releases for faster validation, iteration, and feedback loops.

Compliance & Testing

Built-in QA for HIPAA, ABHA, GDPR, and industry-specific validations.

Deployment & Ongoing Support

Cloud launch, updates, and long-term maintenance with full IP handoff.

Deep Expertise in HealthTech

Deep experience across clinical trials, EHRs, remote care, and real-world evidence platforms.

Full IP Ownership

You own the code, IP, and data — with transparent documentation and dev workflows.

Secure by Design

Follows OWASP standards and modern dev best practices for privacy and scalability.

Why Choose Latent for Clinical Research Software?

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Supported Platforms & Integrations

We Build For

Swift (IOS)

Kotlin (Android)

React Native

Flutter

React (Web)

Vue.js (Web)

Angular (Web)

PWAs

We Integrate With

EHRs

Epic

Cerner

DrChrono

HL7/FHIR

RPM & Wearables

Apple HealthKit

Google Fit

Bluetooth/BLE APIs

Video SDKs

Twilio

WebRTC

Agora

Infra

AWS

Azure

GCP

Payments & CRMs

Stripe

Razorpay

Custom CRMs

Pharmacy Systems

You Bring the Vision. We Bring the Team.

Let’s build your next-generation clinical research platform—faster, smarter, and fully compliant.

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Frequently Asked Questions

How do you handle protocol amendments or mid-study changes in the software?

We design systems with flexibility in mind. Whether it’s updating eCRFs, logic flows, or patient visit schedules, our modular backend allows mid-study changes with minimal downtime—following proper version control and audit trails.

Can your software handle multi-site, multi-country studies with varying compliance needs?

Yes. We support multi-site configurations with country-specific settings like consent forms, language localization, data privacy (e.g., GDPR for EU), and role-based access for different site staff or coordinators.

How do you ensure data validation and reduce entry errors at the source?

We implement real-time form validations, skip logic, range checks, and automated edit checks at the field level. This ensures higher data accuracy before data even hits the backend—reducing downstream cleaning effort.

Can we integrate the platform with our existing EDC or CTMS tools?

Yes. We offer full API-based or custom integrations with leading tools like Medidata, OpenClinica, and Veeva—or build connectors to proprietary systems if needed. We ensure interoperability without locking you in.

What about investigator training and site onboarding—do you support that?

Absolutely. We design intuitive interfaces to reduce learning curves and can also provide training modules, user manuals, or recorded demos to onboard investigators, CRCs, and monitors efficiently.

Is your system suitable for decentralized or hybrid clinical trials (DCTs)?

Yes. We've built platforms that support remote patient enrollment, eConsent, wearable data capture, telehealth visits, and automated reminders—all essential for decentralized or hybrid trial models.

How do you support audit readiness and regulatory inspections?

Our systems maintain complete audit trails, timestamped activity logs, version-controlled forms, and user access reports. We also help prepare documentation for 21 CFR Part 11 and GCP audit requirements.

What happens if we need additional features post-launch—how does scaling work?

Our architecture is designed for scalability. You can start with an MVP and add new modules (e.g., ePRO, RTSM, reporting dashboards) without replatforming. We offer long-term support to grow with your study portfolio.