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.
Popular Posts
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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.
Diabetes to Obesity Drugs | How Ozempic and Mounjaro Became Wegovy and Zepbound
How diabetes drugs took a detour into the world of celebrity weight loss and into the realm of the growing obesity crisis.
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.
Centralizing Clinical Trial Procurement: A Step-By-Step Guide
A step-by-step guide to elevate efficiency, gain control over costs, and seamlessly communicate with stakeholders.
Switching to Centralized Procurement for Clinical Trials
Navigating the complex terrain of clinical trials, shifting to centralized procurement emerges as a strategic odyssey.
Ship Your Next Clinical Trial to Over 100 Locations
Find out exactly where we can ship.
World-Class Import Structuring Can Transform Your Clinical Trial
Surely that’s worth a conversation?