Enterprise Quality Management Software

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:

• Audit Management:Plan, manage, and conduct internal or

• 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.

• Change Management: Implement new changes across the entire organization and make them stick.

• Complaint Management: Streamline customer complaint handling and regulatory reporting through the Events module.

• Deviation Management: Capture, do root cause assessment, resolve, and track both supplier and internal manufacturing deviations through Events Module.

• Document Management: Build a foundation for quality management practices and compliance using Document Control Module.

• Out of Specification Management: Perform investigations of out-of-specification events.

• 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?

• 21 CFR Part 11

• EU Annex 11

• GAMP 5

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.

Related links:

• The advantages of a cloud based eQMS over paper based QMS systems

• 8 reasons why you should turn your paper-based QMS into an eQMS

• Choosing a 21 CFR Part 11 compliant QMS