Featured Articles on Global & FDA Regulation
EUDAMED is moving toward mandatory use. Ensure your medical devices are registered by the 2026 deadlines. Learn about UDI data, XML uploads, and Swissdamed requirements.
Discover why thousands of FDA-regulated food facilities trust Registrar Corp's PCQI training. FSMA-compliant, auditor-approved, and taught by global food safety experts.
The Changing Landscape of Standards of Identity (SOIs) — What Food & Beverage Companies Need to Know
The FDA is revising decades-old Standards of Identity, starting with pasteurized orange juice. Learn what’s changing, the pros and cons for manufacturers, and how to prepare for the impact on labeling, compliance, and consumer trust.
Latest Global & FDA Compliance Articles
Many food exporters to U.S. assume they are in FDA compliance based on past successful shipments. But FDA and FSVP compliance may not be in place, crating risk.
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Managing EMA ASMF submissions can be complex. Learn how pharmaceutical companies simplify Active Substance Master File procedures & regulatory management.
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Ensure smooth U.S. entry with inspection-ready FSVP documentation—reduce import delays, avoid Import Alerts, and protect long-term market access.
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Safety training costs in manufacturing go beyond fees—weak training drives incidents, downtime, turnover, and insurance risk. Learn true cost of skipping.
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Avoid FDA API and bulk ingredient shipment detentions. Learn common registration, listing, and NDC errors—and how Registrar Corp helps keep imports compliant and moving.
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