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.
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.
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.
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.
Our IOR Project Management comes with: