Clinical trials can often involve numerous cross-border shipments. When combined with the complexities of different international regulatory bodies, the management of shipments can be extremely time-consuming for clinical trial coordinators, investigators and other healthcare professionals.
Biocair oversees every detail of clinical trial logistics operations. Our knowledge, global network and expertise ensure we deliver fully compliant, comprehensive and tailored logistics solutions for your clinical trial. Whether that involves shipping individual biological samples or a dedicated trial supply chain with collection and delivery across multiple continents.
Patients may be at the end of the clinical trial supply chain, but they are central to every decision we make at Biocair.
Our patient-centric approach drives our research and innovation, enabling our experts to develop new supply chain and logistical solutions to support the future of clinical trials and personalised medicine, such as cell and gene therapy.
With extensive experience handling and transporting biological goods, potentially hazardous and other sensitive materials, our team always puts the needs of the patient first.
Biocair provides full visibility and real-time tracking information throughout the clinical trial supply chain, including temperature and GPS location, across all our service offerings.
Our trusted global network benefits from a thorough understanding of cross-border logistics.
With over 35 years of expertise, Biocair is the first choice for personalised, GDP compliant clinical trial supply chain management, wherever you are based.
Biocair’s team of experts ensures documentation and records are accurately handled throughout shipping, maintaining product viability to its final destination.
Biocair provides complete management of your clinical trial logistics, with a tailored approach that delivers added value throughout the supply chain – helping you with on-site packing, facilitating shipments through customs and last mile delivery.
With Biocair’s enhanced communication and management, 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.
To discuss your clinical trial supply chain management and logistics requirements, contact our team today.
Multinational pharmaceutical company, Philadelphia (US)
Increasingly complex and global clinical trials have led drug developers to collaborate with logistics experts to manage their clinical trials supply chain.
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.
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.
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.
Wherever you are located in the world, our team of experts are on hand to support your supply chain.