IMPO / Clinical Trials
Investigational Medicinal Products Online
IMPO Core Features
- Centralizes drug accountability workflow
- Eases the process of data retrieval
- Precise product traceability
- CFR 21 Part 11 Compliance
The IMPO (Investigational Medicinal Products Online) system serves as a highly specialized drug accountability tool engineered for managing a company's investigational medicinal products.
It refines how clinical teams retrieve complex product data, establishing absolute drug accountability while supporting instant, real-time tracking across active distributions.
This tool is an integral part of ITClinical's pharmaceutical portfolio, embedding our core corporate philosophy: making life easier for our operational partners.
By complying with regulatory requirements for electronic systems, the platform seamlessly replaces paper-based recording metrics.
- Collaborate online for faster feedback loops
- Access your data from anywhere at any time
- Reduce overall clinical trial data management time
Platform Highlights & Deep-Dive Details
Advanced visual asset management for investigational product batches.
Products and separate batches can be added, monitored, and audited effortlessly within the IMPO system structure. The database archives essential operational parameters, including raw manufacturer variables and exact environmental storage condition rules.
Unitary Batch Traceability
Once a product asset is recorded, users can track and log individual product or device shipments. This enables complete, continuous unitary traceability of explicit dosage forms or hardware devices throughout their lifecycle. Granular database queries can be executed to isolate transaction records immediately.
Integrated Document Attachments
Extra source documentation can be mapped directly to any drug accountability record panel. This provides immediate workspace access to external packaging configurations, manufacturing manifests, or patient leaflet updates.
Automated Shipment Manifest Generation
Compliant product shipment profiles and delivery sheets can be generated dynamically on the fly, formatted perfectly for inclusion inside physical delivery cargo boxes.
Clinical Trial Association
The system features an integrated Clinical Trial management module. By connecting basic study metadata parameters, explicit medication sets or unique medical devices can be linked, filtered, and queried per unique protocol identifier.
Replacing manual paper registers with fully transparent, validated tracking modules.
The IMPO design framework satisfies rigorous international electronic record directives by shifting physical asset tracking into automated logs.
System-Wide Audit Trails
A continuous, chronological tracking register automatically saves every modification, input, and data verification state with precise user credentials and time signatures, making the system fully audit-ready.
Role-Based Credential Gateways
A flexible multi-tier permission matrix limits visibility and transactional authority to designated organizational groups, ensuring strict protocol enforcement across all supply chain actions.
Tailoring systems around your technical environment and operational roadmap.
We analyze your trial's specific scope and supply structure to deliver highly customized, cost-effective deployments rather than pushing rigid, overbuilt packages.
Technology Infrastructure Flexibility
Deploy the platform directly onto your secure internal corporate server architecture via complete Technology Transfer, or rely on our fully managed, high-availability secure Cloud instance.
The platform runs on enterprise-level Linux server instances, which removes scaling limitations and zero out software licensing costs for your operations.