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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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See Our Work in Action

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.

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.

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.

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.

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.

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.

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) – Disease Registryg ALS – Remote Clinical 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

Formly (Tata Memorial) – Disease Registryg ALS – Remote Clinical 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.

Clinical Trials Management Software (CTMS)

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

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.

Electronic Data Capture (EDC)

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

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.

Remote Patient Monitoring (RPM)

Integrate wearables and mobile sensors for continuous vitals tracking.

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.

Health Data Collection Platforms

Scalable platforms to manage high-volume clinical data sets.

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.

Disease Registry Systems

Custom registry tools with longitudinal patient tracking and analytics.

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.

Non-Invasive Diagnostic Tools

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

Non-Invasive Diagnostic Tools

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

Let’s Talk About Your Use Case

Our Process: From Idea to Industry-Ready Platform

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.

Let’s Talk About Your Use Case

Deep Expertise in HealthTech

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

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.

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.

Secure by Design

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

Why Choose Latent for Clinical Research Software?

Connect With Our Product Expert

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

Clinical Research Software Development

Custom Clinical Research Software, Built for Precision and Compliance

Why Top CROs and Research Teams Choose Us

Clinical-Grade Expertise

Clinical-Grade Expertise

End-to-End Compliance

End-to-End Compliance

Plug-and-Play Integrations

Plug-and-Play Integrations

MVPs in 4 to 8 Weeks

MVPs in 4 to 8 Weeks

Full Lifecycle Support

Full Lifecycle Support

Flexible Pricing Models

Flexible Pricing Models

Client Success Stories in Clinical Research

Formly (Tata Memorial) – Disease Registryg ALS – Remote Clinical Platform

Formly (Tata Memorial) – Disease Registryg ALS – Remote Clinical Platform

Tailored Solutions for Clinical Research Software

Clinical Trials Management Software (CTMS)

Clinical Trials Management Software (CTMS)

Clinical Trials Management Software (CTMS)

Electronic Data Capture (EDC)

Electronic Data Capture (EDC)

Electronic Data Capture (EDC)

Remote Patient Monitoring (RPM)

Remote Patient Monitoring (RPM)

Remote Patient Monitoring (RPM)

Health Data Collection Platforms

Health Data Collection Platforms

Health Data Collection Platforms

Disease Registry Systems

Disease Registry Systems

Disease Registry Systems

Non-Invasive Diagnostic Tools

Non-Invasive Diagnostic Tools

Non-Invasive Diagnostic Tools

Our Process: From Idea to Industry-Ready Platform

Discovery & Requirements Mapping

UX/UI Design

Agile Development

Compliance & Testing

Deployment & Ongoing Support

Deep Expertise in HealthTech

Deep Expertise in HealthTech

Full IP Ownership

Full IP Ownership

Secure by Design

Secure by Design

Why Choose Latent for Clinical Research Software?

Supported Platforms & Integrations

EHRs

RPM & Wearables

Video SDKs

Infra

Payments & CRMs

You Bring the Vision. We Bring the Team.

Frequently Asked Questions

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

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

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

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

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

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

How do you support audit readiness and regulatory inspections?

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

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

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

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

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

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

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

How do you support audit readiness and regulatory inspections?

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