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Clinical Manufacturing

Our Competencies

Your development partner from preclinical through phase III

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 

  • Packaging design
  • Process design
  • Formulation support
  • Feasibility and stability studies
  • Technical and clinical batches
  • Scale-up for Phase III
  • Regulatory support

Why trust your clinical supplies to Vetter

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

Contact us

How can we help? We offer extensive contract development and manufacturing expertise. To discuss your next project or request more information, connect with us.

Get in touch