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Clinical trial supply services

Nuvisan has over 40 years of experience providing clinical trial supply services, offering a comprehensive range of solutions. These solutions include regulatory consultancy, manufacturing services, packaging and labelling, randomisation list creation, analytical testing, just-in-time labelling and distribution, comparator sourcing, storage and worldwide distribution, return and destruction services, direct-to-patient shipments, compassionate use and expanded access services as well as controlled drug handling. 

 
Two operators placing capsules on the tray of a blistering machine

Manufacturing of IMP

Nuvisan offers formulation development and manufacturing services for a quick entry into phase 1. No matter if you favor the exploratory formulation approach for the simplest possible formulation or a commercial formulation approach, we support your development needs. Our scientists offer development of semi-solid topical and oral liquid formulations, including a reliable strategy to reduce risks on scaling-up and strong support considering the industrial transfer for future commercial stages. 

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Primary packaging of capsules in bottles

Primary and secondary clinical packaging

Primary and secondary clinical packaging at Nuvisan is a critical component of our clinical trial services, helping ensure the safe, compliant and efficient handling of investigational medicinal products (IMPs). Nuvisan addresses your specific clinical packaging needs, by offering packaging into blister cards, wallets and customised patient kits, combining different products needed for the application and/or take-home medication.

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Labelling a vial into an insulated box before proceeding to shipment

Global logistics management

Nuvisan offers comprehensive solutions for the logistics, storage and management of clinical trial materials, helping ensure seamless support for your clinical trials. Our services align with the highest standards of compliance and efficiency. Our GMP facilities feature controlled access and are humidity- and temperature-monitored. Qualified storage capacities are available for ambient conditions, as well as refrigerated (2-8°C), frozen (-20°C) and ultra-low temperature (-80°C) storage. 

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Two people working together hand in hand

Overall clinical-supply project management

Nuvisan’s clinical-supply project management provides end-to-end oversight of the project thanks to coordination across manufacturing, packaging, labelling, distribution and reconciliation. Our expert teams help ensure GMP/GDP compliance, global regulatory alignment and timely delivery.

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Two printed documents are placed on a table for regulatory review

QP release

All GMP activities are done under the supervision of on-site EU qualified persons (QPs). Our six full-time qualified persons are well-experienced to release various types of finished products (oral, topical, sterile and biological drugs as well as vaccines and blood products) according to European GMP standards.

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