For more than 25 years, Vetter has been on the market as a worldwide leading independent specialist in the contract manufacturing of pre-filled application systems with FDA approved products, employing FDA-approved processes. Vetter Development Service supports pharmaceutical and biotech customers from the early stage of product development to its launch. Vetter Commercial Manufacturing (Contract Manufacturing) handles the entire process from compounding and aseptic filling to the final packaging of a product. Vetter Solutions’ patented application systems, including appendant production services, enable its customers a competitive edge worldwide.
Vetter: FOYA Category Winner Process Innovation
Vetter was awarded the 2007 Facility of the Year Award in the Process Innovation category for its new facility Ravensburg Vetter South (RVS). The international jury of experts selected RVS for its technical innovations that have been optimally designed to meet the existing and future demands of the pharmaceutical manufacturing of prefilled syringes, cartridges and vials. RVS features maximum automation. The production site currently has two filling lines for liquid and lyophilized drugs, both equipped with the Restricted Access Barrier System (RABS). One line has been designed for dual-chamber syringes and cartridges, the second for single-chamber cartridges and vials. Thanks to perfect modularity, two more lines can be implemented even while the first two are running.
Download the Ravensburg Vetter South (RVS) brochure for more information about the facility.
For all North American questions, please use the following contact information:
Vetter Pharma-Turm Inc.
Heston Hall/Carriage House Suite 203
1790 Yardley-Langhorne Road
Yardley, PA 19067
Phone: 215-321-6930
Fax: 215-321-6932
E-Mail:
info@vetter-pharma.com
Download the company brochure for additional information about Vetter Pharma.
Featured Papers
Uncertainty In Process Control — The Limit Of Setting Limits
Although test procedures used in pharmaceutical quality control have to be validated, these validation experiments are usually performed in early development stages in special laboratories using special equipment by specially skilled analysts. This may lead to an underestimation of the procedure's variability and the setting of inappropriate — in most cases too tight — specification limits.
Know-How Technology Transfer From R&D To Manufacturing
Each product needs to be transferred from R&D scale to commercial manufacturing scale. This requires precise project planning at an early stage, a competent project team, a sophisticated application system, and a filing strategy which meets the time-to-market approach.
