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.
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.
We had developed the modules including
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…
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.