USP Broadens <1663>/<1664> E&L Scope for SUS Parts: learn how the 2026 revision reshapes extractables and leachables compliance, supplier qualification, and export readiness for U.S. and EU bioprocessing markets.

Single-use bioprocessing consumables Europe outlook for 2026: explore supply risk, validation burden, regional sourcing shifts, and cost drivers shaping smarter biologics buying decisions.

USP dual standard update puts SUS bags under mandatory USP <665> and USP <1665> compliance. Learn the 2027 FDA PAI impact, E&L file requirements, and key supplier actions now.

EU EPR rule adds mandatory fees for bioreactor bags from July 1, 2026. Learn how EPR registration affects EU customs, CE workflows, supply chains, and market access.

EU EPR Rule Adds Fees for Bioreactor Bags: learn how the 2026 EU EPR change affects registration, customs clearance, OEM exports, and landed costs for EU-bound shipments.

Extractables and leachables testing explained through USP standards: learn key requirements, risk assessment principles, and how robust E&L programs protect safety, compliance, and product quality.

Bioprocessing equipment selection directly impacts scale-up success. Learn how process fit, validation, single-use strategy, and supply resilience can reduce risk and protect timelines.

Single-use bioprocessing vs stainless systems: discover what really changes in cost, validation, contamination risk, and supply resilience to make smarter manufacturing decisions.