Download our brochure to help you comply in critical production environments

For organizations that manufacture and supply infant formula, review and compliance visits from regulatory bodies such as the US Food and Drug Administration (FDA) are inevitable, and in recent years have increased, with some labs being inspected at least twice yearly.

Meanwhile, many labs are not able to easily locate and provide evidence to demonstrate adherence to validated processes or have appropriate checks in place.

Thermo Scientific SampleManager LIMS software can help infant formula manufacturers to adhere to processes and reduce the risk of being issued a Form 483 by the FDA.

Find out how, by downloading our brochure.

 

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