EOR
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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.
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.
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.
Centralized vs Decentralized Procurement for Clinical Trials: The Supply Chain’s Battle Royale
Centralized vs decentralized procurement and finding the best supply chain solution for your clinical trial.
Ukraine Medical IOR | Crucial Patient Data From a Conflict Zone
Navigating trade compliance and medical IOR for a shipment of eCOA devices from Ukraine, a conflict zone. The case study examines how conflict-zone disruptions and strict dual-use regulations stranded a CRO’s clinical trial devices in Poland. It details how TecEx Medical resolved the complex post-Brexit compliance hurdles to safely deliver the shipment from Ukraine to the UK.
Ensuring VAT Compliance in Clinical Trials: The Vital Role of IORs
To avoid legal and financial repercussions, IORs play an essential role in guaranteeing adherence to VAT regulations.
Streamlining the Clinical Trial Supply Chain: Ensuring Innovation Efficiency
The clinical trial supply chain and the importance of streamlining supply chain management.
Clinical Trial Imports into Sweden
Key challenges for importing to Sweden and how an expert medical IOR can ensure a successful outcome.
World-Class Import Structuring Can Transform Your Clinical Trial
Surely that’s worth a conversation?