Implementing a corrective action software system is the first step to effectively managing the CAPA processes within a life science company. FDA and EU regulations require companies to document and track CAPA processes from the beginning to the resolution to ensure the quality and safety of their products. MasterControl Inc.’s corrective action software solution, MasterControl CAPA™, combines time-tested technology with the dynamic experience of technical and customer support teams to help companies increase customer satisfaction, product quality, and ensure regulatory compliance.

About MasterControl Inc.
MasterControl Inc. is a leading provider of GxP process management systems helping regulated life science companies automate, streamline, and effectively manage every stage of the product development lifecycle. MasterControl™ suite includes a continuum of integrated applications, including corrective action software solutions, that are easy to use, easy to deploy, easy to validate, and easy to maintain. Hundreds of companies worldwide use MasterControl for faster compliance, faster validation, and better GxP process management.

White Paper Downloads

	White Paper Download: MasterControl CAPA
	Product Data Sheet: Does Your CAPA need a CAPA
	White Paper Download: How to Kick-Start Your CAPA Process

Kick Start CAPA Processes with Time-Tested Corrective Action Software
MasterControl’s corrective action software offers real solutions to the major challenges of CAPA implementation. MasterControl CAPA™ offers the following solutions to address the problems of inefficiency, disconnected processes, and a lack of visibility within the corrective action system of a company:

• Efficient System: automates routing, delivery, escalation, and approval of CAPAs and all related documents. Also, provides a centralized repository for all documents, making search and retrieval easy during inspections and audits.
• Connected Processes: integrates the CAPA process with the rest of the GxP process system. This connectivity means that a CAPA form can be launched directly from another form, such as a customer complaint, to streamline the process. 
• Automatic Tracking: tracks all routing information and data entered into the electronic best practice form, allowing the nonconformance owner to identify bottlenecks and understand the sequence of events during processing.

Find the Information to Make the Right Decisions about Corrective Action Software
MasterControl is dedicated to providing the educational and research materials life science companies need to make the right decisions about corrective action software.

• MasterControl’s Education Centre is a comprehensive site featuring industry white papers, tech papers, case studies, Q&As, online demonstrations, and corrective action software product data sheets. Here, regulated companies can find answers to their questions about GxP process management software solutions.
• GxP Lifeline is MasterControl’s complimentary monthly newsletter published specifically for life science companies across the sectors of the industry. This virtual space encourages education, training, and collaboration among life science companies with feature stories; sector-specific articles; best practice tips; and, a current listing of life science conferences, events, and trade shows.

Contact MasterControl Today
MasterControl Inc. provides corrective action software that goes beyond software to provide real solutions to the challenges of FDA compliance. To learn more about the integrated, easy to use corrective action software, MasterControl CAPA™, contact MasterControl online or call toll free at 1.800.825.9117 to speak with a representative.

Related Items:

• Corrective Action Preventive Action
• Corrective Action Contract
• Corrective Action System
• Corrective Action Industry Software
• Preventive Action Handbook
• Preventive Action
• Adverse Drug Event
• CAPA
• FDA Guidelines