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
FDA Announces New Medical Device User Fees for FY 2027 beginning October 1, 2026. Compare registration, 510(k), De Novo, and PMA fees.
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Here's how organizations can rethink their approach to food manufacturing training and adopt modern solutions that scale with operational demands.
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Your CPSR must be fully compliant with the EU’s 82‑allergen rule. See what Safety Assessors check — Part A & B, exposure math, MoS, and red flags.
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Don't rely on IFRA certificates alone. Learn how to request 82-allergen data from fragrance suppliers before July 31, 2026 — with a copy-paste template.
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Compare the original 26 EU fragrance allergens to the expanded 82-allergen list under Regulation (EU) 2023/1545. Formulator's deep-dive + free review.
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