What We Do

At VIVUNT Oncology, we offer Contract Development Manufacturing services, specialized in sterile oncology medicines in liquid and lyophilized forms, in vials, applying state-of-the-art technology.

Our Technology

We comply with the highest standards in the industry,
supported by the certification of the new EU GMP Annex 1.

Installed Capacity

Our pharmaceutical site has been built under the highest standards in the
industry and equipped with state-of-the-art technology.

3 production reactors with capacity to manufacture batches ranging from 3
to 900 liters.

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Legislation

We strictly comply with current legislation on manufacturing regulation and we follow international standards and guidelines, applicable to the pharmaceutical industry. We rigorously adhere to the agreements included in product licenses and marketing authorizations, ensuring that all documentation submitted for registration before health authorities complies with the highest quality standards. Moreover, we implement the requirements derived from internal documents issued by the Corporate Quality Direction and Quality Assurance of the group´s sites, which reflects our commitment to excellence and to our products´ safety.