Clinical Manufacturing
The period from preclinical through phase III is sometimes unpredictable for new molecules. With Vetter, you have a partner you can trust to support you throughout drug product development, clinical manufacturing and regulatory approval. We are ready to provide clinical fill and finish for different batch sizes and with a variety of injection systems, from vials, syringes and cartridges. Take advantage of our ongoing investment in technology and quality and our comprehensive know-how in
Extensive expertise in complex, sensitive compounds
With facilities in Germany and the US we offer scalable processes
Regulatory experts are well versed in the required approval processes with global authorities
Our experts help you create a flexible, efficient and scalable manufacturing process.
Key steps include compounding, filtration, preparation of primary packaging materials, and filling.
A wide range of analytical services designed to allow quick-release analytical testing of your clinical material.
Vetter works with you through all phases of regulatory submission.
Learn more about how we can support your clinical success
How can we help? We offer extensive contract development and manufacturing expertise. To discuss your next project or request more information, connect with us.