Document compliance is essential to sustaining regulatory compliance in the stringently regulated FDA and EU environments. MasterControl Inc. provides the GxP process management software solutions to help regulated life science companies attain document compliance across an enterprise.

About MasterControl Inc.

MasterControl Inc. is a leading provider of GxP process management software solutions. For over a decade, MasterControl has been at the forefront of the GxP process management industry designing software specifically for FDA and EU regulated companies. With time-tested document compliance software solutions and the dedicated support of technical and customer services, it is no wonder over 400 companies around the world choose MasterControl GxP process management software to sustain regulatory compliance.

Document Management Dowloads

	White Paper Download: Automating Document Control Processes in FDA and ISO Environments
	White Paper Download: Standard Operating Procedure ( SOP ) Management as a Compliance Tool in FDA and ISO Environments
	White Paper Download: 21 CFR Part 11 - Are You Ready for an FDA Inspection?
	White Paper Download: 21 CFR Part 11 - Risks of Noncompliance

Simplify the Document Compliance Environment with MasterControl GxP Process Management Software Solutions

MasterControl Documents™ includes the following features to help companies optimize the document compliance environment and sustain compliance:

1. Automation of all GxP process tasks such as routing, escalation, review, and approval of documents and forms.
2. Connected solution for holistic quality management by allowing the exchange of files and data between other MasterControl software applications, including CAPA, training, and change control.
3. Robust analytics and reporting capability for effective management and complete document compliance with FDA and EU regulations.
4. Supports change and growth on three levels: users, business units, and operations. MasterControl's document compliance software solutions is an off the shelf, scalable, configurable, and flexible solution.
5. Integrates training for a complete approach to GxP process management, so any change to a document or process that requires new training will automatically launch training tasks upon approval.
6. Continuous validation strategies for sustaining document compliance to reduce the time, pain, and cost involved in software validation.

MasterControl Documents™ is the core application in MasterControl suite offering a complete approach to document compliance that is integrated, time-tested, and easy to use.

GxP Lifeline—A Virtual Space for Education and Research

Each month, MasterControl publishes GxP Lifeline—a complimentary online newsletter dedicated to discussing the latest FDA and EU regulation news. GxP Lifeline is a virtual space where life science companies come to find feature articles and stories about sustaining regulatory compliance, document compliance and GxP process management software, and the latest life science events, including conferences, trade shows, and more.

For More Information

Life science companies must compete in a continually evolving and competitive atmosphere. MasterControl's Education Centre is a comprehensive site dedicated to providing the industry's latest educational and research materials, so FDA and EU regulated companies can make the right decisions about managing document compliance.

To learn more about a complete approach to managing all GxP processes employed by MasterControl's document compliance software solutions, contact MasterControl online or call toll free at 1.800.825.9117 to speak with a representative.

Related Items:

• Enterprise Document Management
• Document Control Training
• FDA Regulatory Compliance
• GXP
• Benefit of Document Management System
• Document Control Procedure
• Digital Document Management Software
• Document Control Management