Pharmpur offers comprehensive, customized manufacturing of medical devices under one
In our new company building state-of-the-art cleanrooms with flexible production systems are available for contract manufacturing. A customized zone concept meets international standards.
Proven methods of aseptic filling in accordance with ISO 13408-1, combined with validated
methods of steam and heat sterilization, represent the basis for the manufacture of medical
devices for the CE market in accordance with DIN EN ISO 13485:2003, medical devices
and drugs in accordance with 21 CFR 820-QSR for the US market, and in accordance with CAN/CSA-ISO 13485-2003 for the Canadian market.
Safe and efficient contract manufacturing of pharmaceutical products calls for considerable experience and systematic implementation of the highest quality standards. Our excellently
trained specialists work strictly according to validated methods of manufacturing and production.
Liquids and high-viscosity media in a volume range from 0.5 - 20ml can be filled (higher volumes
on request). A modular system permits the selection of product-oriented primary packaging from
a portfolio of various prefilled syringes, vials and stoppers.
Final packaging / labeling of the finished goods is semiautomatic or manual, as requested by
As a manufacturer of CE-approved products, Pharmpur also offers manufacturing with identity certificate. The product is placed on the market by the customer and Pharmpur is the product manufacturer.