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Overall clinical supply project management

End-to-end clinical supply project management

Nuvisan offers comprehensive clinical supply project management, overseeing the entire lifecycle of clinical trial materials. From manufacturing and packaging to global distribution and inventory management, our expert team helps ensure timely, compliant and efficient delivery. With a focus on quality, regulatory adherence and customised solutions, Nuvisan supports clinical trials from start to finish, optimising supply chain performance.

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Corporate project management

At Nuvisan, our corporate project management (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. 

Led by certified professionals with PRINCE2 and PMP credentials, our CPM team coordinates cross-functional efforts across Nuvisan’s sites in France and Germany. Acting as the central interface between clients and operational teams, we help ensure strategic alignment, streamlined communication and efficient execution. 
 
With a structured approach rooted in best practices, our CPM team expertly manages timelines, mitigates risks and optimises resources while maintaining strict adherence to regulatory requirements. 

Our certified project managers bring a depth of knowledge across the pharmaceutical value chain, from drug discovery to clinical development, helping ensure high-quality end-to-end solutions tailored to your objectives. Their qualifications and commitment to excellence help ensure superior service delivery, project success and guidance throughout your entire project.

Drug return, accountability and destruction

At the end of the clinical trial, we organise your drug returns from the clinical sites, perform the drug accountability according to your specific level of detail (e.g., dosage form count/kit count/usage) and provide you with the appropriate reports. After receiving your approval, we organise the qualified destruction and associated destruction verification reports are issued. We offer these services globally.

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Email us

hello@nuvisan.com

Talk to us

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+49 731 9840 0 

Our locations

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Neu-Ulm (headquarters)

Wegenerstrasse 13

89231 Neu-Ulm

Germany

Berlin

Muellerstrasse 178

13353 Berlin

Germany

Sophia Antipolis

2400 route des Colles

06410 Biot

France

Grafing

Am Feld 32

85567 Grafing

Germany

Waltrop

Im Wirrigen 25

45731 Waltrop

Germany

For concerns about pharmaceuticals or adverse drug-related events, contact us at: complaints@nuvisan.com
 
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