Nuvisan’s experienced EU qualified persons (QPs) oversee all GMP activities conducted at our facilities. We offer QP services for both investigational and commercial products, as well as importation services, including third-country audits and acquisition of import permits to support global supply chain operations.
All GMP activities are executed under the direct oversight of EU qualified persons (QPs) situated at our two GMP-certified facilities. Our six full-time QPs are highly experienced in the release diverse finished medicinal products including oral, topical, sterile and biological drugs, as well as vaccines and blood derivatives, in strict compliance with European GMP regulations.
Whether you need QP services for investigational, compassionate use/expanded access or commercial products, we can meet your requirements.
To facilitate the importation of medicinal products into Europe, we also offer the qualification of third-country manufacturing and testing sites through audits, and the issuance of the QP declaration and application for import permits. Our professional QPs are experienced and knowledgeable in global supply chain evaluations.
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