What We Do
At Vinvunt Pharma 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 development pipeline includes 10 sterile oncology medicines.
Our Technology
We comply with the highest standards in the industry,
supported by the certification of the new EU GMP Annex 1.
Quality Control & Microbiology.
Fully-equipped laboratories for the analysis of raw materials and finished products, including APS and stability chambers.
Automated In-Process Control (IPC).
The IPC system guarantees the quality in each step of the manufacturing process.
Continuous monitoring of Class A & B.
Filling level control by dynamic scale.
Automated vial crimp capping.
Ensuring an hermetic and safe sealing for each vial.
Isolators for sampling/weighing of raw materials for solution manufacturing.
Equipped with precision technology, the isolators ensure a safe and exact handling of APIs and excipients of the manufacturing process.
Automated Solution preparation system.
With CIP, SIP, DIP and filter integrity test, which guarantees sterility in each step of the product manufacture.
Installed Capacity
Our pharmaceutical site has been built under the highest standards in the
industry and equipped with state-of-the-art technology.