We can arrange the contract manufacturing of small batches of investigational materials for phase I and II clinical trials through the manufacturing capabilities.
Coordinated clinical management
We can supervise the formulation, manufacturing and release of these products to multiple locations across Europe, according to your needs.
When required, our skilled teams can also provide you with advice and assistance in completing relevant parts of the regulatory dossier submission.
We can also develop intermediate suspension products, creams and liquid ointments, suspensions and powder-capsule products.
All the contract manufacturing sites we use adhere to Good Manufacturing Practice (GMP) for assurance of quality control and high standards.
Clinical Trial Supply Europe 2017
Meet the Alcura team in Barcelona on 15 and 16 March, 2017, for the 17th Clinical Trial Supply Europe conference
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Contact us for any questions regarding our services. For patient enquiries please contact your local patient services team