Overall clinical supply project management

We offer comprehensive clinical supply project management, supporting all stages from DS to final EU QP certification of a finished drug. From manufacturing and packaging to global distribution and inventory management, our team helps ensure timely, compliant and efficient delivery, with a focus on quality, regulatory adherence and customised solutions that optimise supply chain performance from start to finish.

Our corporate project management (CPM) team is led by certified professionals holding PRINCE2 and PMP credentials. The team coordinates cross-functional efforts across our sites in France and Germany, acting as the central interface between clients and operational teams to help ensure strategic alignment, streamlined communication and efficient execution.

Our CPM team helps ensure a seamless client journey through every stage of pharmaceutical development. From concept to delivery, we transform ideas into results, combining expertise and precision to meet your goals on time, within budget and in scope. With a structured approach rooted in best practices, our team manages timelines, mitigates risks and optimises resources while maintaining strict adherence to regulatory requirements.

At the end of the clinical trial, we organise drug returns from the clinical sites and perform drug accountability according to your specific level of detail, for example, dosage form count, kit count or usage, and provide you with the appropriate reports. After receiving your approval, we organise qualified destruction and issue the associated destruction verification reports. We offer certified destruction services for material stored at one of our Nuvisan sites or at a partnering local depot on a global scale.