G-LSP
Tagname : Droplet Generators
![EU Tightens IVDR Annex I for Microfluidic IVD Imports]( "EU Tightens IVDR Annex I for Microfluidic IVD Imports")
EU Tightens IVDR Annex I for Microfluidic IVD ImportsIVDR 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 Learn how EU changes may affect CE files, clinical evidence, and delivery timelines.![FDA Draft Guidance Expands Validation Scope for Biomanufacturing Lab Equipment]( "FDA Draft Guidance Expands Validation Scope for Biomanufacturing Lab Equipment")
FDA Draft Guidance Expands Validation Scope for Biomanufacturing Lab EquipmentFDA Draft Guidance Expands Validation Scope for Biomanufacturing Lab Equipment, covering new GMP validation rules, ISO 13485 and USP 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.![FDA Tightens E&L Rules for Lab Fluidic Devices]( "FDA Tightens E&L Rules for Lab Fluidic Devices")
FDA Tightens E&L Rules for Lab Fluidic DevicesFDA Tightens E&L Rules for Lab Fluidic Devices: learn how new extractables and leachables guidance impacts Single-Use Bags, Lab-on-a-Chip systems, imports, compliance, and delivery planning.![ECHA Adds Five SVHCs Affecting Microfluidic Device Exports]( "ECHA Adds Five SVHCs Affecting Microfluidic Device Exports")
ECHA Adds Five SVHCs Affecting Microfluidic Device ExportsECHA adds five SVHCs affecting microfluidic device exports to the EU. Learn how droplet generator suppliers should prepare for 2026 supply chain notification and CE-IVDR/MDR compliance.![FDA GMP Update Reshapes Droplet Generator Exports]( "FDA GMP Update Reshapes Droplet Generator Exports")
FDA GMP Update Reshapes Droplet Generator ExportsFDA GMP update reshapes droplet generator exports as Class II rules, biocompatibility validation, and release testing tighten U.S. market access. See what exporters must prepare before October 2026.![ECHA Draft Restriction Adds Compliance Pressure for Droplet Generators]( "ECHA Draft Restriction Adds Compliance Pressure for Droplet Generators")
ECHA Draft Restriction Adds Compliance Pressure for Droplet GeneratorsECHA draft restriction on droplet generators raises REACH compliance pressure for EEA trade. Learn key risks, importer document requirements, and supply chain actions before January 2027.![FDA GMP Update Reaches Lab-on-a-Chip Devices]( "FDA GMP Update Reaches Lab-on-a-Chip Devices")
FDA GMP Update Reaches Lab-on-a-Chip DevicesFDA GMP update now covers Lab-on-a-Chip devices and droplet generators. Learn what the 2027 U.S. export rules mean for validation, biocompatibility, and supplier compliance.![ECHA Adds 3 Nanomaterials to SVHC List, Affecting Droplet Generator Exports]( "ECHA Adds 3 Nanomaterials to SVHC List, Affecting Droplet Generator Exports")
ECHA Adds 3 Nanomaterials to SVHC List, Affecting Droplet Generator ExportsECHA Adds 3 Nanomaterials to SVHC List, directly affecting droplet generator exports to the EU. Learn the 0.1% threshold, SCIP duties, and key compliance steps before January 2027.![ECHA SVHC Update Reaches Precision Fluid Devices]( "ECHA SVHC Update Reaches Precision Fluid Devices")
ECHA SVHC Update Reaches Precision Fluid DevicesECHA 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.![ECHA Adds 12 SVHCs Affecting Lab Fluid Devices]( "ECHA Adds 12 SVHCs Affecting Lab Fluid Devices")
ECHA Adds 12 SVHCs Affecting Lab Fluid DevicesECHA 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.![ECHA Adds 5 SVHCs Tied to Microfluidic Devices]( "ECHA Adds 5 SVHCs Tied to Microfluidic Devices")
ECHA Adds 5 SVHCs Tied to Microfluidic DevicesECHA adds 5 SVHCs tied to microfluidic devices, triggering SCIP notification from Oct 1, 2026. Learn how Glass Reactors, Nano Flow, and Lab-on-a-Chip exporters can avoid EU customs delays.
{item.title}
{item.description}