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The United States Importer of Record Rules Are Changing: Are Your Clinical Trial Imports Protected?
US Customs is overhauling Importer of Record rules under EO 14411, imposing strict vetting, higher bond minimums, and instant holds for incomplete data. TecEx Medical acts as your compliant US IOR, taking the regulatory burden off clinical sites to guarantee zero trial delays.
Importing Radiopharmaceuticals: Import Compliance for Research
When managing the physical decay of therapeutic isotopes, working with an experienced Importer of Record ensures regulatory alignment, minimizes customs friction, and protects the integrity of trial-critical supplies.
Who is Responsible for Importing Clinical Trial Materials?
The entity that acts as the Importer of Record (IOR) depends on who can bear legal, financial, and regulatory accountability.
Double-Blind Study: IOR Clinical Trials
TecEx Medical safeguards double-blind studies because of our speciality in the documentation required for IMP shipments.
The Art of Cutting Costs: Streamlined Clinical Trial Procurement
Optimize cross-border clinical trial procurement by balancing centralized control with IOR frameworks to eliminate customs delays, tax losses, and excess spend.
TecEx Medical’s Import Tax Solution
Pharma sponsors waste money treating import taxes as unavoidable sunk costs. TecEx Medical’s IOR expertise unlocks major savings via VAT reclaims and tariff optimization. Ultimately, proactive tax structuring turns import expenses into a repeatable cost-saving strategy.
Clinical Trial EOR: Exporting IMP, Devices and Samples From Trial Sites
An Exporter of Record (EOR) in clinical trials is just as important as an Importer of Record (IOR). Partnering with a proactive EOR will safeguard your study’s timeline, trial assets, and integrity.
Biotech IOR: Importing Advanced Therapies, Biologics and Lab Samples Globally
Streamline global clinical trial logistics with a dedicated Biotech IOR. Prevent customs delays for advanced therapies, biologics, and lab samples with TecEx Medical.
What Is an Exporter of Record for Clinical Trials?
Ensure cross-border clinical trial success with an Exporter of Record (EOR) to streamline regulatory compliance, prevent customs holds, and safeguard study timelines.
IOR vs EOR: Understanding The Difference in Clinical Trial Logistics
Learn about IOR vs EOR clinical trial logistics and how TecEx Medical ensures customs compliance and regulatory authority expectations are met.
What Is an Importer of Record for Clinical Trials?
Clinical trial IOR is the legal entity responsible for ensuring that medical shipments comply with customs regulations.
Emerging Medical Drug, Technology, and Compliance Concerns
The pharmaceutical sector is rapidly moving, and a recurring pattern of compliance vulnerabilities emerges.
World-Class Import Structuring Can Transform Your Clinical Trial
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