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 and regulatory support
- Process Development: Expertise is the key to manufacturing processes that meet your exact specifications. We can work with you to create processes that are flexible, scalable, reproducible, and efficient.
- Clinical Trial Manufacturing: Our clinical manufacturing capabilities in the US and Europe, combined with our focus on time-to-clinic, can streamline your path to clinical trials. With dedicated project management, we provide the confidence that all the necessary steps for clinical batch release of your compound are completed on time.
- Analytical Services: Our highly-experienced team uses a wide array of innovative analytical techniques to validate all raw materials, bulk solutions, in-process materials, and finished products. Our highly trained analytical quality control staff also provides support for the critical transfer of analytical methods.
- Regulatory Support: We support you in all regulatory phases for both new market entrants and established products. Our in-depth knowledge of global regulatory requirements will help you with regulatory documents that are needed for both clinical studies as well as marketing authorizations for registration.
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