Clinical Trial Management System
End-to-End Trial Management Solutions
Risk based Monitoring Tools
100% Compliance to Global Regulations
CDISC Compliant
End-to-End Trial Management Solutions
Risk based Monitoring Tools
100% Compliance to Global Regulations
Electronic Data Capture (EDC)
21 CFR Part 11 and HIPPA Compliant
Robust Data Validation Checks
Multiple eCRF Collection Tools
Integrated Medical Dictionary
21 CFR Part 11 and HIPPA Compliant
Robust Data Validation Checks
description
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
Glorant LLC d/b/a Octalsoft alternative Software Development Company
