Transforming clinical trial supply chain management

Biocair is the global specialist in clinical trial supply chain management, providing personalized logistics solutions for domestic and international multi-site clinical trials.

Clinical trial logistics

Clinical trials can often involve numerous cross-border shipments. When combined with the complexities of different international regulatory bodies, managing these shipments can be time consuming for clinical trial coordinators, investigators and other healthcare professionals.

Biocair oversees every detail of the operation. Our knowledge, global network and expertise ensures we deliver fully compliant, comprehensive and tailored logistics solutions for your clinical trial, whether that may include a single shipment study, or a multi-site collection and delivery trial across continents.

Biocair clinical trial logistics

Advanced monitoring

Biocair provides full visibility and real-time tracking information, including temperature and GPS location, across all our service offerings.


Global expertise

Our trusted global network benefits from a thorough understanding of cross-border logistics.


Regulatory compliance

With over 35 years of expertise, Biocair is the first choice for a personalized, GDP compliant clinical trial supply chain solution, wherever you are based.

Biocair clinical trial value added logistics
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Value added clinical trial logistics

Biocair provides complete management of your clinical trial logistics, with a tailored approach that delivers added value from collection to delivery – helping you with everything from on-site packing, facilitating shipments through customs and local delivery.

  • 24/7 global coverage
  • Utilization of the most efficient global transport routes
  • Completion of all paperwork and labelling, wherever legally possible
  • Full classification of materials and rapid customs clearance
  • Provision of validated packaging, including on-site packing

Communication and support

With Biocair’s enhanced communication, you have full visibility of your clinical trial materials throughout the supply chain. Our advanced and comprehensive reporting ensures detailed, real-time information is available when you need it.

  • 24-hour Biocair contact
  • Temperature, GPS monitoring and reporting services
  • Advanced preparation of all documentation, ensuring swift customs clearance
  • Local on-site assistance available across our global network

To discuss your clinical trial supply chain management requirements, contact our team today.

Contact us Get a quote

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The Biocair office I work with has provided terrific service. The staff are helpful and always responsive to my questions and requests. This trial involved multiple international sites both inside and outside the EU, as well as shipping multiple sample types that had to be sorted at the clinical sites. The shipments were carried out quickly and without any issues.

Scientific Investigator

Multinational pharmaceutical company, Philadelphia (US)

Case studyBringing innovation to the clinical trial supply chain

Increasingly complex and global clinical trials have led drug developers to collaborate with logistics experts to manage their clinical trials supply chain.

Read more


FAQ icon

Can Biocair arrange collection of blood samples from international clinics participating in our study, and then return them to our facility in a different country?

Yes, Biocair can arrange collection of blood samples and other materials from clinical sites around the world, including supplying the PI650 inner bags for the samples, labelled outer packaging and dry ice.

How can Biocair support me with customs clearance for an upcoming clinical trial?

The first step towards ensuring a smooth customs clearance is to ensure that all required documentation/licensing is included when the material is shipped.

Biocair staff are experienced in ensuring that all documentation is prepared in a manner that accurately describes the material being shipped, while also ensuring that any additional required elements (HTS codes, FDA codes, clinical trial authorization documentation, etc) are also included.

What paperwork and licenses may be required for a clinical trial? How can Biocair support?

The paperwork and licences required depends on a number of factors, including:

• Where is the clinical trial due to be conducted?
• What transport route is required?
• What type of material (s) is involved?

Wherever legally possible, Biocair will provide the required documentation. This includes airwaybills, NES declarations and dangerous goods certificates. All labelling for transport is also provided.

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Get in touch with Jessica

Wherever you are located in the world, our team of experts are on hand to support your supply chain.

Message Jess Get a quote

Jessica Deveau from Biocair

Jessica Deveau

Director of Sales

North America

+1 347 539 4980

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