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Problems with equipment maintenance, cleaning and calibration are among the FDA’s most commonly observed deficiencies. If you want to avoid these issues and reduce risk you need this report.
This authoritative management report offers a comprehensive analysis of the FDA’s regulatory requirements — and more importantly, strategies for complying and reducing risk while saving time and money.
Is your organization at risk of FDA 483s and Warning Letters?
Ideal for Drug and Device Makers
Remember: Requirements to Maintain Equipment are Not Self-Evident – It’s the Details
Rather, they result from an inability to satisfy the detailed requirements of maintaining a defensible maintenance, calibration and cleaning schedule.
In addition to explaining regulatory requirements, this report tells you how to avoid issues associated with frequencies as well as operational limits — and what to expect in the future.
Information You Need From an Expert You Can Trust
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