Tag Archives: FDA

How ESHA Uses and Implements FDA’s Guidance for Industry Documents

We often receive questions regarding how ESHA implements recommendations for compliance from the FDA's Guidance for Industry documents into our software solutions. This blog briefly covers how we regard and use both types of guidance documents that the FDA publishes.

Draft Guidance Documents

Definition: FDA’s draft guidance documents do not...
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Nutrition Facts Label Industry Resources

The introduction of the FDA's new Nutrition Facts Label regulations has stirred up a lot of questions and some confusion. We have compiled this list of resources to help you find the answers you need.

Government Resources

FDA's Overview of Changes The FDA has put together a summary of the changes here, including an FAQ section. This is a good...
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Proposed Label Regulations Sent to the OIRA

On April 29, 2016 the FDA gave the proposed labeling regulations to the Office of Information and Regulatory Affairs (OIRA) (part of the Office of Management and Budget), who will review the guidelines to make sure they are consistent with the applicable law and that they do not conflict with policies and procedures from another...
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