Staying Ahead of FDA Findings with a CMMS
The FDA offers very clear and exacting standards for medical product development and manufacturing, and they’re quick to issue a recall when these requirements are
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The FDA offers very clear and exacting standards for medical product development and manufacturing, and they’re quick to issue a recall when these requirements are
Every facility strives for an environment where equipment is effectively maintained, breakdowns are largely avoided, and operations are safe and accident-free, but few attain it.
The medical device market is booming, and regulated manufacturers are experiencing increased demand and scrutiny around safety practices. Planning ahead is a top priority at
Regulated manufacturers require strong facility management to be successful. These managers are responsible for ensuring smooth day-to-day operations, and they’re also tasked with improving efficiencies
There are sophisticated software solutions available today that can optimize the regulated manufacturer landscape. It’s software that makes maintenance, calibration, and asset management easier, with
Although there’s a big difference between a U.S. Food and Drug Administration (FDA) Form 483 Observation and an FDA Warning Letter, both are nerve-wracking notifications
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