Clinical Trial Logistics

Ensuring proper collection, labeling, packaging, and transportation of biological samples (blood, urine, tissue) from clinical trial sites to testing laboratories while maintaining temperature and chain of custody requirements.

Managing the distribution of investigational drugs, medical devices, and supplies to clinical sites, including temperature-sensitive products that require specialized handling and storage.

Ensuring compliance with regulatory requirements, such as Good Clinical Practice (GCP), Good Distribution Practice (GDP), and local regulations for import/export of clinical trial materials.

Identifying and mitigating risks associated with logistics, such as delays in transportation, temperature excursions.

Leveraging technology solutions like temperature monitoring devices, GPS tracking, and inventory management systems to enhance visibility and control over clinical trial logistics.