Enterprise Quality management software (EQMS) helps life science businesses in the paperless assessment and maintenance of the product or service quality while complying with the regulatory requirements. EQMS is also referred as e-QMS which stands for Electronic Quality Management System.
What can you do using Quality Management Software?
Quality Management Software is helpful for everything that you can do in a paper-based Quality Management System. Scilife is a Quality Management Software too. Quality Management activities that Scilife cloud-based e-QMS handles are as below:
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- Audit Management: Plan, manage, and conduct internal or external supplier and regulatory audits.
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CAPA Management: Implement risk-based corrective and preventive action plans triggered by an Out of Trend, Out of Specification or Out of Expectation Event using CAPAs Module.
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Change Management: Implement new changes across the entire organization and make them stick.
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Complaint Management: Streamline customer complaint handling and regulatory reporting through the Events module.
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Deviation Management: Capture, do root cause assessment, resolve, and track both supplier and internal manufacturing deviations through Events Module.
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Document Management: Build a foundation for quality management practices and compliance using Document Control Module.
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Out of Specification Management: Perform investigations of out-of-specification events.
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Training Management: Ensure a competent and compliant workforce.
To know more about why pharmaceutical and other life science industries require a Quality Management Software read this blog article.
What are Regulatory Requirements that Quality Management Software Must Meet?
Quality Management Software is a great tool that can save the organizational cost of maintaining paper-based Quality Management Processes. Quality Management Software also helps to increase employee productivity and overall organizational efficiency.
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