ValidationMaster™ Portal

Integrated Quality, Risk, and Compliance Solution For Life Sciences

 

Validating computer systems demands a high level of quality and control throughout the process.  During validation exercise, validation engineers generate a significant number of documents as evidence of required due diligence.  As a matter of best practice, a robust, full-featured content management system is essential to the success of the validation project.

 

The ValidationMaster Portal™ is a fully integrated Microsoft SharePoint-based enterprise quality, risk and content management solution.  Tightly integrated with the ValidationMaster™ Enterprise Validation Management system, the ValidationMaster Portal™ manages validation deliverables and helps to effectively address quality and risk management throughout the validation process.   The ValidationMaster Portal™ is compliant with any quality standard including ISO 9001:2015 AND includes the following KEY features:

 

 

Click on the links below to learn more about the rich capabilities and functionality in the ValidationMaster™ Portal.


Nonconformance Management

The ValidationMaster Portal provides a 360 degree view for each quality record.  Key relationships and activities are visible in a single page.

Risk Management

Ensures that risks are identified, periodically assessed tracked and monitored.  Interactive risk matrices and acceptance levels are fully configurable.

Compliance Intelligence

Metrics provide managers with actionable intelligence regarding quality process efficiency.  Interactive dashboards are designed to display charts and data.

Content Management

Comprehensive regulatory document collaboration and control backed by SharePoint®.  Fully electronic route, review and electronic signatures in compliance with 21 CFR Part 11.

Objectives

Define quality objectives and alerts to help drive quality, risk and compliance initiatives.  Define, track and manage key performance indicators for corporate quality programs.

CAPA Management

Manage tasks, documents and a closed-loop CAPA process in a systematic controlled manner to help drive quality throughout the enterprise.

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