Bring your clinical trial to life with TecEx Medical’s experts in trade compliance for the medical industry. We are your go-to IOR and customs compliance partner specializing in clinical trial project management.
The demand for lifesaving innovations and medical devices is increasing around the world, driving the growth of the medical sector in international trade. However, the healthcare industry also remains one of the most challenging aspects of global trade. Companies face many hurdles in this rapidly growing area of the global economy. Complexities such as intellectual property protection, country-specific compliance requirements, logistics, tariffs, licensing requirements, trade agreements, and ethical demands are some of the many challenges faced by those in the clinical trial sector. As a result, supply chain management has become the lifeblood of efficient cross-border medical transactions.
TecEx breathes life into your global clinical trial supply chain with our project management solution.
Stuck shipments of medical supplies and missed Site Initiation Visit (SIV) dates are the worst-case scenario for those conducting cross-border clinical trials.
Yet an estimated 85% of clinical trials experience delays. Regulatory, procedural compliance, and clinical supply chain issues are some of the most common reasons for clinical trial delays.
TecEx Medical’s complete trade compliance and clinical supply chain management solution safeguards your international trials.
| Provide project support
or clinical trials by obtaining regulatory approvals, managing inventory, compliance risk mitigation, and shipping samples. |
Navigate the regulatory requirements
for clinical trials and ensure they comply with all applicable regulations. |
Increase trial efficiency
by streamlining business processes and reducing the risk of delays through a single point of contact. |
| Manage project efficiency
by ensuring complete regulatory import and export compliance in destinations around the world, including China, Mexico, America, and more. |
Avoid costly penalties and delays
by efficiently filing customs clearance documents, paperwork, registrations, and paying duties and taxes on your behalf. |
Provide cross-border expertise
by sourcing and managing regulatory requirements, licenses, and permits. |
| Manage and advise
on various pain points in the supply chain – from regulatory requirements and compliance risk management to time sensitivity and noncompliance penalties. |
Handle administrative responsibilities
from the beginning of your trial through its completion. Our project management solution ensures a more compliant and efficient supply chain. |
Streamline global deployments
by integrating supplier and service provider relationships across the supply chain. |
Provide project support
or clinical trials by obtaining regulatory approvals, managing inventory, compliance risk mitigation, and shipping samples.
Navigate the regulatory requirements
for clinical trials and ensure they comply with all applicable regulations.
Increase trial efficiency
by streamlining business processes and reducing the risk of delays through a single point of contact.
Manage project efficiency
by ensuring complete regulatory import and export compliance in destinations around the world, including China, Mexico, America, and more.
Avoid costly penalties and delays
by efficiently filing customs clearance documents, paperwork, registrations, and paying duties and taxes on your behalf.
Provide cross-border expertise
by sourcing and managing regulatory requirements, licenses, and permits.
Manage and advise
on various pain points in the supply chain – from regulatory requirements and compliance risk management to time sensitivity and noncompliance penalties.
Handle administrative responsibilities
from the beginning of your trial through its completion. Our project management solution ensures a more compliant and efficient supply chain.
Streamline global deployments
by integrating supplier and service provider relationships across the supply chain.
Since cross-border clinical trials and import/export controls are so intricate, enlisting the help of a trade compliance expert can make your trial or clinical investigation quicker and more efficient. TecEx Medical provides a complete cross-border project management solution supporting your clinical trial in multiple destinations from inception to completion. Our value-added services also ensure safe and efficient delivery for your clinical trial.
We’re more than just a consignee — we act as your local and legal representative for importing medical commodities. This means we handle all the paperwork and import requirements for customs clearance so that you can focus on your trial.
We also help with the export of your clinical trial supplies and provide real-time updates regardless of the location of your trial site. This means we can help you retrieve vital clinical trial data quickly and easily.
We apply for all required permits and licenses to import medical commodities. This ensures that your clinical study complies with all source and destination country compliance requirements.
We file customs clearance documents, paperwork, registrations, and payment of duties and taxes – helping you avoid delays and fines. Whether Australia is your importing country or you’re working within the European Union, TecEx is your go-to trade partner.
Find further information about how our project management solution enables clinical trial deployment.