Key benefits: Why eValidation is a game changer
The 2024 State of Validation report found that 61% of validation professionals in highly regulated industries experienced increased workloads due to new products, process changes, and evolving regulatory demands. Traditional validation methods often involve time-consuming manual tasks, lengthy approval cycles, and compliance risks stemming from human error. eValidation offers an automated, scalable solution that aligns with regulatory expectations while enhancing productivity.
1. Ensuring data integrity
Data integrity is a cornerstone of global regulations and is addressed by best practices like ISPE’s GAMP® 5 and the Record and Data Integrity Guide. Robust eValidation systems uphold ALCOA++ principles, ensuring that data is:
- Attributable: Each action is linked to a specific user via secure logins and digital signatures.
- Legible: Eliminates errors and misinterpretations associated with handwritten notes.
- Contemporaneous: Actions are time-stamped, ensuring real-time accuracy.
- Original: Data is captured directly in digital format, eliminating transcription errors.
- Accurate: Built-in validation checks reduce errors and ensure compliance.
- Complete: Automated workflows ensure all required data is captured, preventing omissions.
- Consistent: Standardized templates and workflows maintain uniform data entry.
- Available: Cloud-based access enables authorized users to retrieve records instantly from any location.
- Traceable: Comprehensive audit trails log all actions, ensuring transparency and accountability.
By adhering to these principles, eValidation provides a secure, traceable, and audit-ready system that mitigates compliance risks.
2. Improving efficiency across the validation lifecycle
Validation processes encompass multiple steps, including document authoring, review and approval, test execution, and archiving. EValidation systems significantly reduce the time spent on each stage by enabling:
- Automated document creation and approval workflows: Streamlines the generation and authorization of validation documents.
- Online test execution: Allows for real-time recording of test results, enhancing accuracy and speed.
- Instant digital signatures: Eliminates the need for physical sign-offs, expediting the approval process.
- Real-time collaboration: Facilitates seamless interaction across departments and locations.
- Automated audit trails: Reduces preparation time for inspections by maintaining comprehensive records.
3. Harmonizing validation across multiple sites
Global pharmaceutical companies often face inconsistencies in validation practices across different sites. eValidation fosters a standardized process that ensures:
- Consistent validation procedures: Uniform practices across all locations enhance compliance and quality.
- Simplified compliance monitoring: Centralized systems make it easier to oversee adherence to regulations.
- Automated traceability matrices: Facilitates seamless documentation tracking and retrieval.
A centralized eValidation system breaks down silos, improving coordination between departments and regulatory teams.
4. Reducing deviations and improving right-first-time outcomes
Manual validation processes are prone to deviations due to documentation errors, missing approvals, or inconsistent testing methods. eValidation minimizes these risks by:
- Providing real-time access to the latest protocols and documents: Ensures all team members are working with current information.
- Automating deviation tracking and resolution workflows: Streamlines the identification and correction of issues.
By reducing the likelihood of deviations, eValidation supports a right-first-time approach, cutting down on costly rework and delays.
