MasterControl - Quality Audit Management Software
FDA Audit Preparation
Effective preparation is key to audit management success. Compliance audit management using MasterControl Quality Excellence gives you the assurance that no audit-related activities will be overlooked. For example, automated planning ensures all participants are notified of the event details. Conflict detection identifies and prevents scheduling issues.
Audit Checklists
Your audit checklist is a list of tasks to be completed during an audit. You include this in the audit file. Audit checklist software, like MasterControl Quality Excellence, lets you quickly identify nonconformances. Gain a holistic view of all audit processes, highlight areas of following best practices, and provide evidence of compliance in real time.
Audit Workspace
The audit workspace is where you compile all audit-related information. The audit management team uses the workspace to create the audit report and manage the response collection process. MasterControl Quality Excellence consolidates the workspace contents. This lets all approved stakeholders access the audit data from a centralized location.
Audit Report Creation
Without an effective reporting tool, it’s difficult to create accurate and timely audit reports. Also, more and more companies need to meet global report guidelines. With MasterControl Quality Excellence, you have a single source of truth for all data. You also have the tools to create both localized and global reports in the appropriate languages and formats.
Clinical research is costly and time-consuming. To keep costs down, you need to improve efficiency. Clinical audit management solutions and systems help maximize resources. MasterControl streamlines audits of clinical programs, studies, vendors, sites, and quality events for a complete good clinical practice (GCP) audit effort.
When audit management is not connected to other quality processes, it is difficult to identify and resolve audit findings. MasterControl seamlessly integrates audit management processes with all other quality areas. Easily launch corrective/preventive actions (CAPA), deviations, change control, risk management, supplier audits, etc. Ensure nothing falls through the cracks in gaining compliance.