Audit of Quality

Audit-related forms and processes can be automated from start to finish to ensure an audit of quality

Quality auditing entails GMPs (Good Manufacturing Practices), which stipulate practices for quality assurance auditing for medical device, pharmaceutical, biotech and other high-tech organizations. These practices are by nature compatible with iterative, electronic systems. So why is it that many life science and high-tech organizations still utilize an systems for quality audits that are paper-based? While such systems may generate an audit of quality, it is only after a slow (and often frustrating progression) and many employee hours.

Select the type of audits that apply to you:

GLP Audits, GCP Audits, PV Audits, Vendor Audits, Supplier Audits

General Quality Audits, ISO Audits, GMP Audits

Watch Audit and Automation Videos

Passing Audits and Inspections with MasterControl (3:08)

How MasterControl Makes Your Job Easier (3:50)

Free Audit Downloads
	White Paper: Quality Audit - A Tool for Continuous Improvement and Compliance
	White Paper: The Top 5 Benefits of Electronic GLP Audit Management
	Webinar: Automating Quality Audits for Regulatory Compliance
	Interactive and Live Demonstration: MasterControl Quality Suite Demonstration

Which Solution from MasterControl for an Audit of Quality is Right for Your Company?

Both solutions for quality auditing from MasterControl help companies assure an audit of quality. The focus of each solution for audit quality control differs however, as outlined below:

MasterControl Audit is designed for companies who want to assure quality products and services, and thereby greatly reduce risk. The audit software accomplishes this by helping companies attain and sustain a state of "audit readiness". The software provides system transparency to assure management oversight, and has helped many different kinds of companies around the world meet their quality goals.

MasterControl QAAD Audit is a larger scale solution designed to automate resource management and scheduling, as well as audit management activities like reporting and report responses, activity workflows, advanced CAPA functionality (which enables a CAPA to follow multiple workflows within the same audit), root causes, and other activities.
The built-in flexibility of MasterControl QAAD enables the software to be used in multiple business areas within an organization, each area having its own needs. The ability to define an unlimited number of business areas and raise quality issues across business areas makes the software extremely powerful. MasterControl QAAD Audit is used by over half of the top 20 pharmaceutical companies around the world.

Integration with Other MasterControl Solutions

Either audit program can be easily and seamlessly integrated with the other solutions for quality management from MasterControl to ensure not only audit quality control but an efficient quality system.

Benefits of both systems designed to ensure quality auditing include:

A Web-based System: Makes it possible to access the audit software from virtually anywhere.
Centralized System: Makes it easy to control forms for an internal audit; searching for forms and finding them takes minutes instead of hours.
Automation: Tracking tasks, routing, scheduling, approvals, archival and analyses for an audit of quality are all automated.
Customization: MasterControl provides the flexibility that each unique life science or high-tech company requires.
Reporting: Reporting and analytics capabilities are included with the audit software that MasterControl provides.
Potential Integration: Both solutions can be integrated with other MasterControl solutions, such as document control, CAPA, change control, training management, etc.

For More Information

For more information about how the audit systems from MasterControl generate an audit of quality, please feel free to contact a MasterControl representative.