Regulatory Compliance
Showing 12 of 24
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.
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.
The Art of Cutting Costs: Streamlined Procurement in Clinical Trials
Procurement costs of centralized vs decentralized procurement strategies and how each approach can benefit clinical trials.
Risk Mitigation in Clinical Trials: Centralized Procurement for Global Decentralized Trials
The risks associated with decentralized procurement and how to prioritize risk mitigation in clinical trials.
SIV Date in 2 Weeks | Fast-Track IOR
The urgent import of Patient Recruitment Materials for a global clinical trial’s impending Site Initiation Visit date. The case study examines how meeting a strict 15-day deadline required harmonizing complex US and Israeli pharmaceutical compliance standards. It highlights how overcoming these regulatory hurdles ultimately hinged on seamless multi-vendor coordination to ensure flawless final-mile delivery.
World-Class Import Structuring Can Transform Your Clinical Trial
Surely that’s worth a conversation?