Vetter Commercial Manufacturing

Our experience working for your success: Vetter Commercial Manufacturing

Concentrate and focus your resources. Leave the details of production to us, your specialist and loyal partner. Vetter Commercial Manufacturing can handle everything for you – from the initial stages of sterile through the custom-packaging of your final product.

Fill & Finish:
Since the mid-1970s Vetter has been producing aseptically pre-filled application systems – among them primarily standard syringe systems, cartridge systems and self-patented application systems such as the Vetter dual-chamber systems. All processes and products are tested in compliance with international cGMP standards. To date, the number of client products with FDA approvial stands at 18. Our production employs the complete spectrum of modern aseptic technology, for example Restricted Access Barrier Systems (RABS). As specialists in the handling of sensitive "high-value" drugs we have extensive experience in the commercial production and final packaging of biotechnologically derived drugs and aseptic suspensions.

Packaging Service:
Our comprehensive packaging service includes the labeling and packaging of syringes, cartridges and vials to the finished-product stage. We perform 100% inspections of all printed packaging materials by means of integrated code-reading systems and cameras for reading variable data. We offer precision labeling using graduated labels, blister packaging, mounting of originality closures and the assembly of safety systems against needle injuries. We assist our customers in the selection of secondary packaging materials intended to increase patient friendliness and prevent counterfeiting or tampering, and we lend our support to keep our customers' product launches on schedule.

Pharmaceutical Analysis:
Our analytical Quality Control measures comprise the testing of raw materials, packaging materials, bulk solutions, in-process materials and finished products. We also perform stability testing. Our media systems, cleanrooms and processes are routinely monitored. Our personnel is trained in the state-of-the-art analytical techniques.

Regulatory Affairs Service:
Our regulatory support of our customers extends beyond the approval date of a drug. In parallel with routine production, we assist with regulatory activities such as change announcements or the preparation of variation documentation. We offer qualified and reliable consulting services in regulatory matters and the establishment of annual product reviews in accordance with the respective regulatory requirements.

Dosage Forms:
Syringes, Cartridges and Vials