Blog
Knowledge is the foundation of a resilient global supply chain. As part of our commitment to operational excellence, we monitor the frontlines of international regulatory compliance so our clients don’t have to. Our blogs offer a closer look at regional customs shifts, emerging logistics trends, and evolving compliance laws, ensuring your global clinical strategy remains seamless and fully compliant.
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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.
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.
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.
New Canada CARM System: Challenges for Clinical Trial Imports
Sponsors and CROs operating across borders may have recently encountered new and growing challenges when importing clinical trial materials into Canada.
Clinical Trial Project Management for Global Imports
Clinical trial project management focuses on coordinating the moving parts required to run a study across regions.
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