Clinical Trial
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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.
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.
GLP-1 Import
The GLP-1 import scene is continuously growing, transforming obesity treatment and reshaping global healthcare.
A Look Back at the Covid-19 Vaccine Timeline: What Obesity Drug Trials Can Learn
What obesity drug trials can learn from the rapid trial timeline to rollout of Covid-19 vaccines.
Customs Valuation Methodology of Products
In accordance with the World Trade Organization, TecEx Medical follows its methodology of valuation for customs clearance.
How VAT Reclaim Can Save Your Bottom Line
VAT compliance is a critical aspect of conducting global clinical trials successfully. Collaborating with a medical Importer of Record is pivotal in ensuring compliance with VAT regulations and other import-related tax requirements.
World-Class Import Structuring Can Transform Your Clinical Trial
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