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Importer of Record (IOR) services for clinical trials
Simplify global clinical trial logistics and maintain regulatory compliance with Thermo Fisher Scientific's Importer of Record (IOR) services, available in more than 30 countries worldwide.
The biopharmaceutical industry has expanded its global clinical trial footprint over the past two decades. While this trend has improved patient recruitment and diversity, it has also introduced new operational and regulatory challenges across the supply chain.
Import and customs requirements continue to evolve and can vary significantly from one country to the next. Working closely with an Importer of Record (IOR)—or partnering with a provider that can serve as your IOR—can help streamline the import process.
What is an Importer of Record (IOR)?
An Importer of Record (IOR) is the legal entity responsible for ensuring imported goods meet local regulatory requirements. Key responsibilities include:
- Ensuring imported goods comply with local laws and regulations
- Filing customs documentation and required import declarations
- Paying applicable expenses such as import duties, taxes, and fees
Thermo Fisher Scientific provides Importer of Record (IOR) services in more than 30 countries worldwide. Supported by our global network of strategically located cGMP facilities and in-country regulatory experts, we help simplify complex global supply chains.
Download the fact sheet to learn how Thermo Fisher's Importer of Record services can support biotech and pharmaceutical companies conducting clinical trials.
