Glorant LLC d/b/a Octalsoft

About Glorant LLC d/b/a Octalsoft

Multiple eCRF Collection Tools
INTERACTIVE WEB RESPONSE SYSTEM (IWRS) Centralized Patient Enrolment Implement Complex Randomization Schemes Emergency Unblinding 24/7 real- time Access
Implement Complex Randomization Schemes
24/7 real- time Access
Remote Source Data Verification (rSDV) Easy Document Upload and View Standardized Document Repository Source Data Confidentiality & Privacy Secure Environment with Controlled Access
Remote Source Data Verification (rSDV)
Easy Document Upload and View
Source Data Confidentiality & Privacy
Secure Environment with Controlled Access
Portfolio & Project Management Improved Project Governance Predictive Modelling Tools Real time Project Insights Collaborative Problem Solving
Portfolio & Project Management
Real time Project Insights
eDOCS Dynamic Review and Approval Process Document Version Control Electronic Signatures Online Collaboration
Dynamic Review and Approval Process
Electronic Trial Master File (eTMF) Based on DIA TMF Reference Model Centralized Database of Essential Trial Documents Role based Controlled Access All time Audit Readiness
Electronic Trial Master File (eTMF)
Based on DIA TMF Reference Model
Centralized Database of Essential Trial Documents
Role based Controlled Access
All time Audit Readiness
CLINICAL TRIAL SUPPLY MANAGEMENT (CTSM) Clinical Supplies Depot Management Real Time IP Inventory Management Stock Control Instant Drug Accountability
Clinical Supplies Depot Management
Real Time IP Inventory Management
BIOREPOSITORY MANAGEMENT SYSTEM Biospecimen Inventory Management Annotated Clinical Data Powerful Retrieval and Reporting Capacity Configurable Workflows
Powerful Retrieval and Reporting Capacity
Electronic Patient Reported Outcome (ePRO) Software Patient Centric User Interface Realtime Access to PRO Data Secure and Encrypted Bring-your-own device Compatible
Patient Centric User Interface
Realtime Access to PRO Data
CLINICAL TRIAL SOLUTIONS Clinical Trial Management System End-to-End Trial Management Solutions Risk based Monitoring Tools 100% Compliance to Global Regulations CDISC Compliant Electronic Data Capture (EDC) 21 CFR Part 11 and HIPPA Compliant Robust Data Validation Checks Multiple eCRF Collection Tools Integrated Medical Dictionary INTERACTIVE WEB RESPONSE SYSTEM (IWRS) Centralized Patient Enrolment Implement Complex Randomization Schemes Emergency Unblinding 24/7 real- time Access Remote Source Data Verification (rSDV) Easy Document Upload and View Standardized Document Repository Source Data Confidentiality & Privacy Secure Environment with Controlled Access Portfolio & Project Management Improved Project Governance Predictive Modelling Tools Real time Project Insights Collaborative Problem Solving eDOCS Dynamic Review and Approval Process Document Version Control Electronic Signatures Online Collaboration Electronic Trial Master File (eTMF) Based on DIA TMF Reference Model Centralized Database of Essential Trial Documents Role based Controlled Access All time Audit Readiness CLINICAL TRIAL SUPPLY MANAGEMENT (CTSM) Clinical Supplies Depot Management Real Time IP Inventory Management Stock Control Instant Drug Accountability BIOREPOSITORY MANAGEMENT SYSTEM Biospecimen Inventory Management Annotated Clinical Data Powerful Retrieval and Reporting Capacity Configurable Workflows Electronic Patient Reported Outcome (ePRO) Software Patient Centric User Interface Realtime Access to PRO Data Secure and Encrypted Bring-your-own device Compatible