The Authority in Global Agricultural Chemistry & Bio-Resources

FDA eases import path for 12 botanical extracts, cutting Prior Notice and sampling for USP-NF compliant batches. Learn how this update affects exporters, buyers, and GMP-driven market access.

FDA adds GMP declaration rule for Food Grade Enzymes entering the U.S. Learn the new import document requirements, delay risks, and key compliance steps for exporters and buyers.

GMP compliance for vendor comparison: learn what to check before shortlisting suppliers, from certificates and audit readiness to red flags that impact quality, traceability, and supply security.

GMP compliance in batch production starts with strong control points, clear records, and validation discipline. Learn how to reduce audit risk and improve batch quality readiness.

ANVISA opens a fast-track remote GMP review for China agrochemical manufacturers, enabling temporary certification in 8 working days for Brazil registration and customs clearance.

ANVISA opens a fast-track remote GMP review for China agrochemical firms. Learn who qualifies, the 8-day certificate timeline, 50-company cap, and what it means for Brazil registration.

FDA Sets New Import Filing Bar for Food Enzymes: learn how the 2026 FDA import guidance raises GMP and enzyme activity documentation standards, and what suppliers, importers, and buyers should do now to avoid detention risk.

Botanical Extracts exporters face a new FDA pre-entry rule for U.S. shipments. Learn the 72-hour filing, HPLC/UPLC, heavy metal, and GMP requirements to avoid detention delays.