Streamline your clinical operations and make clinical research easier
We are a true cloud venture that provides collaboration in clinical research between sponsors, CROs, and clinical sites by varied range of clinical solutions.
Accelerate clinical data capture with the right insights
Our connected suite accelerates data capture with a real-time centralized solution, monitors compliance and meets regulations on time and within budget.
Overcome challenges, Uncover
new paths
Get your clinical trial back on track with our time-trusted tools and services.
Explore Our Offerings
that puts you on the fastest path to success
We innovate and deliver amazing product line we constantly strive to enhance
our offerings that satisfy clients’ needs.


Computer System Validation of Compliances
Healthcare and Clinical trial application validation for compliances like PII, PHI, HIPAA, SOC2, 21CFR, Data Privacy 11 etc. End-to-End Regulatory & Compliance Management
Design, Installation, Operational and Performance Qualification (DQ, IQ, OQ, PQ)
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Cloud Migration, Application Monitoring & Management
Cloud Migration and Compliance
24x7 Clinical Trial and Healthcare Application Monitoring, Maintenance
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System Integration, Data Migration, Extraction & Curation
Systems Integration with Applications in Healthcare and Clinical Trial Ecosystem and third-party applications Including Financial Applications and Inventory Tracking system
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System Setup for study startup and Pharmacovigilance
Study Setup for EDC (including Design Studies for EDC, CRF Creation, Edit Checks and Assessment Schedule) & Pharmacovigilance System and Safety Signal Management Systems setup
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Professional and Consulting Services
Team of SMEs, Solution Architects, Business Analysts, Frontend and Backend Developers (React JS, Python, Full Stack) and QA for quick Clinical Trial Applications ramp up.
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Application Implementation, Migration & Upgrade Services
Development, Implementation & Maintenance of Clinical Operation Management Applications (Veeva Vault, IQVIA Trial Management and Data Analytics Suites, & Oracle & custom applications)
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Analytics, AI/ML, eCOA, Trial Supply Tracking and Management
Clinical trial Feasibility Study, Outcomes prediction, real-time material tracking etc.
Schedule a Discussion with the ExpertsOne Of The Innovative And Leading Clinical Research Services And Technology Solution Providers
Offering our Customers a Full Spectrum of Professional
and Managed Services
Our commitment is to ensure that clinical trials are both safe and expedient, simplify your regulatory affairs, and assist you with managing quality and learning activities.

Clinical Operations
CTMS
eTMF
EDC
eCOA
RTSM

Regulatory Information Management
Registrations
Submissions
Submissions Publishing
Submissions Archival

Quality Management
System
QMS
Quality Docs

Learning/Training
Management System
Curriculum management
Quality event management
Quality lab operations – SOPs, CC forms

Unique Perceived Benefits With Us
`Supports you with prospective, ongoing and retrospective management of clinical trials
Provides unified access to various stakeholders participating in clinical trials
Streamlines clinical trial operations with a smart and efficient document management system
Manages master data for contacts, sites etc., using our master data management system
Monitors and gains complete visibility and control over all clinical processes
Significant reduction in the study set-up time, increased accuracy of auto-classification, and reduced reconciliation time.
Why Smart IMS
24/7 Monitoring and maintenance of your clinical applications with real-time notification on process and services disruption or failure.
Cost effective Opex & SaaS model and customized Capex model for application services fitting in your requirement and budget.
Experience and expertise to streamline the process and capitalize on cross-departmental efficiencies.
From site identification to Study close-out, we oversee and manage complete clinical operation.
Fully Compliant Solutions with 21CFR Part 11, Annex 11 and HIPAA regulations
Improved site/study management aligned to amendments, protocol, and subject deviations.
Diverse team of clinicians, medical, technology experts and process engineers to help run your trials and manage the processes, site and patient data.
