This course provides a practical introduction to the legal and operational requirements for transporting biological materials in clinical research. Participants will learn the key national, EU, and international regulations, including IATA and ADR, that govern safe and compliant transport. The course explains how to classify biological materials correctly, assess transport-related risks, and apply appropriate packaging, marking, and documentation standards. It also covers biosafety principles, emergency response procedures, and the training and qualification requirements for personnel involved in shipment processes. In addition, participants will gain an understanding of regulatory oversight, including the role of the Civil Aviation Authority.

By the end of the course, learners will be able to implement compliant transport procedures that support safety, regulatory adherence, and good clinical research practice, helping ensure that biological materials are handled and shipped responsibly, efficiently, and in accordance with applicable legal requirements.

AI tools were used to support the technical production and editing of the course. All substantive content, including the script and educational materials, was prepared by the SME.