EN ISO 11607-2:2026 now mandates new Tyvek lid testing for EU medical device exports. Learn the 90-day retesting, CE file update, and compliance risks before shipments are delayed.

USP <665> revision reshapes export requirements for SUS bioreactor bags, highlighting new extractables validation, third-party risk reports, and urgent compliance steps for U.S. and Canada market access.

Life science supplier solutions global strategies help biopharma and diagnostics teams reduce scale-up risk, protect quality, control COGs, and strengthen supply continuity.

Cold chain stability testing cost in 2026 depends on protocol design, sample load, assays, packaging, and compliance. Learn what raises budgets fastest and how to control spend without weakening evidence.