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Stay up-to-date on regulatory developments. Here you’ll find the latest in compliance news and guidance for all our client industries.

Featured Articles on Global & FDA Regulation

Latest Global & FDA Compliance Articles

FDA Drug Amount Reporting: The Deadline You Can’t Ignore

Don’t risk public exposure on the FDA’s noncompliance list. FDA Drug Amount Reporting is now enforced under Section 510(j)(3) of the FD&C Act.

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The MoCRA Unified Agenda: Turning FDA’s Delay Into Competitive Advantage

FDA’s MoCRA delay isn’t downtime—it’s opportunity. Learn how to turn Unified Agenda uncertainty into a lasting competitive advantage.

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Life After De Minimis: How Importers Must Adapt to the New Customs Reality

De minimis is gone. Every shipment now faces duties and FDA scrutiny. See how importers can adapt fast—or risk costly delays and refusals.

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How to Get FDA Approval

Do food, medical devices, drugs, and cosmetics need FDA approval? Read our guide on how to get FDA approval for your regulated product.

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SQF Edition 9 Requirements: What Training Must Practitioners Now Complete?

Edition 9 of the SQF Code redefined what it means to be “qualified.” If your training predates the new standard—or lacks proof—you may face non-conformance. Learn what auditors expect, why old credentials fall short, and how to update your training before your next audit.

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SQF Practitioner Requirements Have Changed—Are You Still Qualified?

If your training isn’t current—or your records can’t prove it—you may not be allowed to lead. Learn what’s changed, what no longer counts, and how to close the compliance gap before your next audit.

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