Does Your CAPA System Need a CAPA - White Paper

The release of FDA's most recent guidance, Quality Systems Approach to Pharmaceutical Current Good Manufacturing Practices (CGMP) reinforces the importance of implementing an effective CAPA process as a critical component in an overall quality system. However, most organizations do not taken advantage of today's technology relying upon manual systems or antiquated technology to handle this significant regulatory process.

The white paper discusses the different approaches for handling CAPA systems and how using proven technologies enable organizations to improve product quality while at the same time meet regulatory requirements. Topics include:

-- Why CAPA?
-- Paper Approach
-- Hybrid Approach
-- Electronic Software Solutions
-- Benefits

Watch Videos How MasterControl Makes Your Job Easier (3:50) Creating a Paperless Process Using MasterControl (3:38)

Downloads:

	Product Data Sheet: MasterControl CAPA - Summary of Features and Benefits
	Product Tech Paper: MasterControl CAPA - Detailed Technical Features and Functionality
	White Paper: Does Your CAPA System Need a CAPA?
	White Paper: Change Control - Quality Improvements in FDA and ISO Environments
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