The SOLABS QM10 Collaborative Review enables Life Sciences organizations to collaborate on controlled documents in real time while maintaining compliance with GxP and data integrity requirements. By providing a single, controlled source for document authoring and review within Microsoft Word, the solution reduces version-related compliance risks, accelerates document approvals, and enhances audit readiness—all within a validated quality management system.
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Supports GxP-compliant document management
Enables controlled authoring and review of GMP, GCP, and GLP documents while maintaining data integrity and procedural compliance. -
Improves data integrity (ALCOA+)
A single, controlled document source reduces the risk of incomplete, inconsistent, or overwritten data, supporting ALCOA+ principles. -
Reduces compliance risk from version errors
Eliminates uncontrolled local copies and manual document merging, minimizing the risk of using incorrect or outdated versions during audits. -
Audit-ready collaboration
Real-time visibility into reviewer changes improves traceability and accountability during document review cycles. -
Faster SOP and controlled document approvals
Accelerates review and approval of SOPs, policies and other controlled documents, and quality records without sacrificing control. -
Enhances inspection readiness
Centralized, controlled documentation supports quicker retrieval and clearer evidence during regulatory inspections. -
Validated system alignment
Designed to operate within a validated SOLABS QM10 environment, supporting Life Sciences quality system requirements. -
Maintains control during cross-functional reviews
Enables collaboration across QA, Regulatory, Manufacturing, and Validation teams without compromising document governance.
For more information of the Collaborative Review feature, please email us at info@solabs.com
A podcast episode on this feature provides more information.
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