Project Management of Global Clinical Trial Imports

21 June 2024

Global logistics and customs compliance issues do not have to be your burden while trying to manage a clinical trial. Focus on more important aspects, like patient recruitment, while we project manage the global deployment of your clinical trial commodities.



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Project Management for Seamless Global Clinical Trials


Our specialist IOR mapping tool ensures full vendor alignment for your study with little involvement from you. Sit in on calls while we handle the shipment and all the compliance needed to get your equipment across borders.


IOR Project Management for Global Clinical Trials

Reduse Lead Times for Regulatory Approval | Mini Case Study


Considering any of the LATAM countries for your next clinical trial? 

In general, Regulatory Approvals (RA approvals) from the MOH can take anywhere from 2-3 months. With looming SIV dates, lead times like this can significantly impact your study. 

Through our IOR Project Management Protocol, we work around our clients’ time expectations and expected RA approval dates to facilitate all compliance and ensure we are ready to ship to achieve SIV dates.

Want to know more?


By including TecEx Medical before the start of the study, we can work together to minimize risks and decrease lead times. Utilizing our trusted Protocol, our end-to-end solution ensures you will always meet your SIV dates.


TecEx Medical’s IOR Project Management solution includes:

  1. Importer of Record
  2. Customs compliance
  3. Customs brokerage and clearance
  4. Logistics
  5. Tax reclaim (if applicable)
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