Importer of Record services: Simplifying your clinical trial imports

Seamless and compliant entry into key global markets 

 

Navigating the complex regulatory landscape of importing investigational medicinal products (IMPs) and clinical trial materials can be a major roadblock in your biotech research. 

 

At Alcura, a Cencora company, we simplify this process. Offering expert Importer of Record (IoR) services, we help ensure smooth and compliant entry of your materials into key markets worldwide, including the European Union.
 

Your trusted Importer of Record

An Importer of Record is a legal entity based in your destination country that assumes responsibility for ensuring all imported goods follow local laws and regulations. 

As your IoR, we handle all necessary documentation, customs clearance, and regulatory compliance activities to allow you to focus on your core research and development activities.

Key markets served

We offer comprehensive IoR services across these regions:

Europe

(including the EU, UK, and Eastern Europe)

USA
Asia
Africa

Why choose Alcura as your IoR?

Global expertise

We help you navigate the complexities of import regulations in key markets across Europe, the USA, Asia, and Africa. With specialized knowledge of the EU market, we help streamline your entry into this complex regulatory landscape.


Streamlined processes

Save time and resources with our efficient customs clearance, documentation, and compliance procedures.


Quality assurance

Trust our rigorous quality control throughout the importing process to safeguard your clinical trial materials.


Peace of mind

Rest assured that your clinical trial materials are imported legally and compliantly, minimizing risk and ensuring the success of your study.

Partner with Alcura

Get in touch with our expert team below to start the journey to simplifying your clinical trials.

Client testimonials

“I would like to extend the congratulations to Alcura and the depots involved in this study. We had our 100th patient randomised today! Thank you to everyone for all the hard work… Keep up the good work.”

Supply Chain Manager, CRO

“I see a lot of emails, and your level of customer service, responsiveness to our team, etc. is great. Keep up the really good work. It’s noted and appreciated.”

Director – Clinical Trial Supplies, CRO

“Thank you for the update and all the efforts you and your team are putting into getting supplies to Ukraine, (during war conflict); it is greatly appreciated!”

Associate Clinical Supply Chain Manager, CRO

“This is a job very well done. Congratulations!”

Founder and Managing Director, Sponsor

Meet our team

Our leaders rely on their unique backgrounds and expertise to foster a global mindset that guides our dedication to patient care all over the world.