In the case of ancillary products used in global clinical trials, the EOR ensures that the products meet the regulatory requirements of the country where the trials are taking place.
This can include:
• Obtaining approval from the local regulatory body,
• Ensuring that the products are labelled and packaged correctly,
• Complying with safety, health, and environmental standards.Contact Us
TecEx Medical assists with navigating the customs clearance process and complying with all relevant trade regulations, identifying and mitigating supply chain risks, and ensuring that products are delivered on time and in good condition.
Furthermore, we provide guidance on the local regulatory requirements, obtain necessary permits or licenses, and ensure that all compliance documentation is correct and in order. This will ensure that the trial runs smoothly without any compliance-related interruptions.
With our expertise and experience, you can trust us to take care of all the compliance complexities, while you focus on the clinical trial.