Diagnostic imaging equipment manufacturer evaluation guide: learn how to compare service depth, system integration, compliance readiness, and lifecycle cost for smarter procurement decisions.

EU imported ultrasound devices face a new MDSAP rule from October 2026. Learn how the EU compliance shift affects exporters, distributors, supplier reviews, and market access planning.

Diagnostic Imaging systems comparison made practical: explore MRI vs CT vs ultrasound for clinical use, workflow fit, cost, and procurement decisions to choose smarter imaging solutions.

FDA Tightens 510(k) Filing for AI Imaging Modules: learn how the new FDA rule impacts AI imaging submissions, validation packages, pending 510(k) reviews, and launch timelines.

Suez Canal surcharge pushes ultrasound shipping costs higher, adding about $1,450 per TEU. See how this impacts medical equipment pricing, delivery planning, and buyer budgets.

Carriers prioritize ultrasound cargo at Rotterdam with 24-hour discharge priority. Learn how EU MDR Annex XVI pre-declaration now shapes medical equipment shipping, customs speed, and delivery planning.

Dental technology certification shapes real market access. Learn which ISO, IEC, MDR, and FDA standards matter most to reduce delays and expand with confidence.

Diagnostic imaging equipment manufacturer evaluation guide for hospital projects. Learn how to compare compliance, delivery, installation, service, and lifecycle cost with confidence.

Yangshan Port opens a medical device fast-track, cutting clearance to 48 hours. See how faster customs can boost export reliability, delivery planning, and global shipment confidence.

FDA Tightens 510(k) Filing for AI Imaging Devices: learn how the new FDA 510(k) rule affects AI-enhanced X-ray, CT, and MRI submissions, validation packages, timelines, and U.S. market access.

SFDA Sets 72-Hour Imaging Import Filing Rule: learn how Saudi Arabia’s new 72-hour e-SFDA filing and calibration record requirement can affect customs clearance, compliance risk, and delivery timing.

Saudi SFDA opens a fast track for imaging device registration, cutting review time to 25 working days for eligible CE and ISO 13485:2025 certified products. See who benefits now.