S T R A T E D G E   I T

CONSULTING

Welcome to StratEdge IT Consulting, where innovation meets expertise in the realm of digital transformation. We specialize in a comprehensive suite of services tailored to meet your business needs.

Contact Info

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Clinical SaaS Development

All Services

Opening Hours

  • Mon - Sat: 10.00 AM - 7.00 PM
  • Sat: 10.00 AM - 4.00 PM
  • Sunday: Closed
  • Emergency: 24 hours

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+1(302) 232-2218
Clinical SaaS

Clinical SaaS Development

We develop robust, scalable, and compliant SaaS platforms for clinical and pharmaceutical industries. Our solutions simplify trial management, patient engagement, data analytics, and reporting while ensuring full adherence to regulatory frameworks such as FDA, HIPAA, and GDPR.

SaaS Benefits

Benefits With Our Service

Why Clinical Organizations Choose Our SaaS Platforms

  • Clinical Trial Management Systems (CTMS)
  • eSource & eConsent Platforms
  • Regulatory Compliant SaaS Architecture (FDA, HIPAA, GDPR)
  • Multi-tenant SaaS Deployment
  • Real-time Analytics & Reporting Dashboards

From protocol design to real-time data tracking, our Clinical SaaS systems empower research teams and CROs to innovate faster and operate smarter. You gain improved efficiency, better compliance, and actionable insights at scale.

Clinical Platform UI
Dashboard View

Frequently Asked Questions

We follow FDA 21 CFR Part 11, HIPAA, and GDPR compliance standards in architecture, access control, audit logging, and data handling. Each deployment undergoes rigorous validation.
Yes, we offer seamless API-based integration with popular CTMS, EMR/EHR systems, third-party analytics, and trial management solutions.
Absolutely. Our systems are designed for multi-site, multi-tenant setups with permission-based access and centralized monitoring dashboards.
Yes, we customize workflows, forms, user roles, dashboards, and reporting modules based on your specific clinical research or pharma requirements.