Clinical trial logistics at the highest level: Krieger offers GDP and GMP-compliant solutions for investigational medicinal products, including temperature-controlled transport, EU QP release, return management and customised additional services.

Returns management and the safe disposal of unused or expired IMPs are key components of successful trial logistics. We offer safe and efficient return processes that comply with regulations and ensure complete documentation. We also ensure the environmentally friendly and compliant disposal of IMPs in accordance with all regulatory requirements, thereby complying with the highest safety and environmental standards. Complete documentation of all returns and disposal processes ensures compliance and full traceability at all times.

Additional Services

In addition to logistics, we offer a range of tailor-made additional services to optimally support your clinical trial. These include design and label translation to meet the requirements of international trials. We provide suitable packaging materials and handle the packaging of IMPs to ensure their safe and compliant shipment. Customised packaging solutions are developed to meet the specific requirements of IMPs and guarantee the highest safety standards.

We rely on comprehensive security protocols and robust risk management to prevent theft, tampering or loss of IMPs. Measures such as access controls, video surveillance and alarm systems reliably prevent unauthorised access to storage areas. In addition, well thought-out emergency plans and effective risk management ensure a fast and efficient response to incidents such as transport damage, delays or temperature deviations to guarantee the safety of the products at all times.

Clinical trials often require adjustments during implementation. We offer flexible and scalable logistics solutions that adapt to changing needs. Thanks to scalable services, we can react flexibly to changes in protocol, the opening of new trial centers or fluctuating volumes. In addition, individual logistics processes are developed that are specifically tailored to the requirements of your clinical trial to ensure smooth and efficient execution.