What is Octalsoft?

Octalsoft offers a comprehensive suite of cloud-based, AI/ML-enhanced eClinical software solutions that are purpose-built to facilitate efficient, secure, and compliant management of global clinical trials. The platform integrates advanced technologies to accelerate drug discovery, patient selection, trial design, and real-time monitoring, supporting industry stakeholders such as pharma companies, CROs, biotech firms, hospitals, and medical device organizations.

With capabilities spanning Clinical Trial Management Systems (CTMS), Electronic Data Capture (EDC), Interactive Web Response Systems (IWRS), ePRO, eTMF, supply management, and analytics, Octalsoft empowers users to centralize operations, ensure regulatory compliance, and achieve operational excellence. The modular architecture and agile development approach ensure each deployment aligns with specific client needs, supporting decentralized trials, process automation, and seamless data management across multiple therapeutic areas and geographies.

Features

Cloud-Based CTMS: Centralizes operational and study data for real-time visibility and control across global trials.
AI/ML Integration: Enhances drug discovery, patient selection, trial design optimization, and real-time monitoring.
Electronic Data Capture: Streamlines collection and management of patient data for early to late-stage clinical studies.
Interactive Web Response System (IWRS): Facilitates subject enrollment, randomization, and investigational product supply management.
ePRO Platform: Provides encrypted, regulation-compliant patient outcome reporting with automated reminders.
Electronic Trial Master File (eTMF): Enables customizable, wizard-driven document storage and regulatory compliance.
Supply Management: Tracks and optimizes inventory, ensuring regulatory compliance and seamless logistics.
Decentralized Trial Support: Powers virtual clinical trials with tools for remote management and participant engagement.

Use Cases

Managing multi-site global clinical trials for pharmaceutical sponsors.
Automating data capture, patient reported outcomes, and compliance for CROs.
Optimizing investigational product inventory and logistics in medical device studies.
Streamlining regulatory document management for biotech clinical research.
Supporting decentralized/virtual clinical trials post-pandemic.
Enabling hospitals to securely track, analyze, and manage clinical trial data.
Enhancing transparency, speed, and accuracy in drug discovery and development processes.