Global Lab-Scale Production & Fluidic-Precision (G-LSP)

G-LSP

Tagname : Syringe Pumps

China Tightens Export Compliance Checks on Lab Fluid-Control Devices
China Customs tightens export checks on lab fluid-control devices, requiring CE/UKCA compliance docs and labels. Learn how the new rules may delay shipments and affect global sourcing.
China Tightens Export Checks on Lab Fluid Devices
China Tightens Export Checks on Lab Fluid Devices: Learn how new CE/UKCA compliance rules from 2026 may affect syringe pumps, pipettes, export clearance, lead times, and global buyers.
China Customs Tightens Export Checks for Lab Liquid-Handling Equipment
China Customs tightens export checks for lab liquid-handling equipment from Sept 2026, requiring CE/UKCA documents and machine-readable labels. Learn how exporters can avoid shipment delays.
EU Tightens IVDR Annex I for Microfluidic IVD Imports
IVDR Annex I update puts microfluidic IVD imports under stricter Class C rules. Learn how EU changes may affect CE files, clinical evidence, and delivery timelines.
How to Select Microfluidic Pumps for Lab-on-a-Chip Flow Control
Microfluidic pumps for lab on a chip selection starts with flow control needs, not catalogs. Learn how to compare pressure stability, pulsation, bubbles, compatibility, and integration for better system performance.
FDA Draft Guidance Expands Validation Scope for Biomanufacturing Lab Equipment
FDA Draft Guidance Expands Validation Scope for Biomanufacturing Lab Equipment, covering new GMP validation rules, ISO 13485 and USP <1058> requirements, and 2027 compliance impacts for suppliers.
ECHA SVHC Update Reaches Precision Fluid Devices
ECHA SVHC Update reaches precision fluid devices: learn how syringe pumps, droplet generators, and Lab-on-a-Chip exports can meet SCIP and EU compliance rules before October 2026.
FDA Tightens Accuracy Rule for Lab Fluid Devices
FDA tightens accuracy rules for lab fluid devices, cutting tolerance to ±0.8% and adding ISO 8655-5:2025 testing. See how suppliers can protect U.S. market access.
ECHA Adds 12 SVHCs Affecting Lab Fluid Devices
ECHA adds 12 SVHCs impacting Syringe Pumps, Droplet Generators, and Lab-on-a-Chip exports to the EU. Learn the new SCIP compliance risks, material review priorities, and actions companies should take now.
FDA Tightens Import Rules for Syringe Pumps
FDA Tightens Import Rules for Syringe Pumps: learn how the 2026 FDA update affects GMP/GLP imports, NIST-traceable calibration certificates, customs clearance, and on-time delivery.
FDA Tightens Syringe Pump Import Checks
FDA Tightens Syringe Pump Import Checks: learn how the new IEC 62443-3-2 validation rule affects customs clearance, retroactive shipments, and delivery timelines to the U.S.
FDA sets full-range syringe pump verification rule
FDA sets full-range syringe pump verification rule, requiring third-party accuracy testing for 510(k) filings. Learn the compliance impact, cost risks, and export planning steps before Oct. 1, 2026.

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