We are providing ICTMS.

Integrated Clinical Trial Management System for management of your trial.

We are providing many moving parts of the clinical trial process; we can monitor progress from a central dashboard. ICTMS manages the clinical trial right from the start and maintains Project and Profile specific access controls across the system, from study design to throughout close-out and regulatory submission. This end-to-end clinical trial management solution includes the tools to plan, startup, conduct, and manage your study, and complete monitoring and regulatory compliance activities. It supports every study aspect, whether design, procedures, protocol, study arms, visits, forms, treatments, payment, and more…

Get an in depth look at ICTMS’s robust features and functions.

Online synopsis, online Feasibility, online MSA – Master Service Agreement, online CTA – Clinical Trial Agreement.

You can online create, share, take review and comments and publish the Content for respective stake holder

About Us

We are a Unit of "Life Research Centre and Strategic Business Unit Private Limited". We are providing tailor made solutions in Clinical Trial Office Automation services and CTMS. We are software & consulting company super specialized in pharmaceutical research.

We provide software automating business processes to CROs and Pharma companies. We combine traditional standard functions for general management in the organization with functionality specific to clinical research.

We developed a web based software platform which allows us to quickly evolve, add new functionality and accommodate client’s requirements.

Features of ICTMS

CRO and Sponsor can Monitor and supervise the study online…

We had developed the modules including

  • Project Management for CRO
  • Project Management for Site
  • Employee Training
  • Create Project Budget
  • Online CDA and Feasibility
  • Online MSA and CTA
  • Site Management
  • Asset Management
  • Study Team Management
  • Supply Chain Management
  • Investigator Database
  • Trial Master File
  • Site Master File
  • Travel Desk Management
  • Electronic Case Report Form – E CRF
  • Investigational Product - IP Development Life Cycle
  • Site Payment system
  • Vendor Management
  • Vendor Payment
  • Expense Management
  • Task Management
  • Mile Stone Guided Project Management
  • Randomization


Benefits of Technology

  • Freedom in hosting model choice
  • Industry competence
  • Integration
  • Customization
  • Value for money

21 CFR Part 11

We follow the 21 CFR Part 11 regulations from the Food and Drug Administration (FDA). We follow the guidelines of security and audit trail for computerized systems used within clinical trials. We are maintaining…

  • User access control
  • Time-stamped audit
  • Keeping of e-records
  • E-signatures
  • Archiving
  • External security safeguards

We are confirm meeting 21 CFR Part 11 technical requirements by employing procedures and controls that include Computer System Validation as per GxP functions to ensure accuracy, reliability, integrity, legibility and consistent intended performance.

General Manager get logged in with credential

Select the allocated Project

Add the Mile Stone as per the project development he want to see. (Select the Mile Stone from drop down list and he can also add the new tailor made Mile Stone)

Project Manager get logged in with credential

Select the allocated project

Update the status of the Project – Mile Stone with date (Select the Status from drop down list and he can also add the new tailor made Status)


Current Openings…

.net developers - 2

Web designers - 2

Send your CV with cover letter to career@liferesearchcentre.in

Request for Demo…

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