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Repeatable, documented processes are critical for GxP compliance. Your quality records set expectations for how processes and tasks should be conducted. Trial Interactive provides a central, controlled workspace to add quality record templates and track them through draft, review, and approval before making them effective. Seamlessly send your records to the GlobalLearn LMS to train teams on clinical trial records to enforce quality compliance.
Simplify QA Record Processes
Ensure GxP and GMP Compliance
Automate Quality Record Processes
Improve Collaboration
Maintain Complete Audit Trail and Record History
Manage Record Versioning
Control Access to Clinical Trial Records with Edit and Read-Only Permissions
Reduce Costs with Centralized Records and Training Management
Monitor Record Processes with Real-Time Oversight
Track Training Progress, Compliance, and Completion
Certify Team Members on Quality Processes through Training Management
Publish Quality Records Directly to the eTMF
Publish Training Certifications to the eTMF
Ethris moved its SOPs and training records from paper-based processes into Trial Interactive Quality Document Management, connected to its LMS. Staff no longer need in-person signatures or manual follow-up, and the company has a clear path to digitizing its full quality operation as it grows.
Quality assurance teams can manage standard operating procedures, policies, and any other records from approved templates as required by the quality manual. Author, edit, approve, and manage quality records.
Simplify quality knowledge management by connecting quality document processes to your training management.
Draft from Template, Edit and Collaborate on Document
Approve with eSignature
Share Approved Document to Training Management
Document Becomes Effective
