Control software aids FDA compliance
A
Control-See Software Solutions product story
Edited by the Engineeringtalk editorial team
May 15, 2006
The latest version of the U.C.ME-OPC software product introduces compliance with the FDA's 21 CFR part 11 legislation.
Control-See Software Solutions, a leading provider of alarm notification and analysis software tools, introduces compliance with FDA's 21 CFR part 11 for its U.C.ME-OPC software product version 6.0.
The FDA is stepping up regulatory enforcement, and achieving compliance is no small task.
Its scope extends beyond a company's environmental and production control systems and operating procedures into virtually every area of the plant and across entire regulated industry supply chains.
Today's biotech, pharmaceutical and other FDA-regulated industries are quickly realising the importance of 21 CFR Part 11 compliance.
They're viewing Part 11 not as a burden, but as an opportunity to improve their manufacturing process and their entire business.
By moving to a fully "paperless" environment, companies can reduce costs, accelerate time to market, and ensure a higher degree of quality and consistency in their products.
As a result, these companies gain a powerful competitive advantage.
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