Your advantage as a VP customer
Safety and quality in medical packaging - Made in Germany
We have been developing and producing medical packaging for more than 40 years. Our customers include large and small companies of the medical device industry in Germany and 70 other countries worldwide.
Innovation is the focus of our business. We maintain our own development department with state-of-the-art equipment ranging from the tensile testing machine to the FTIR spectrometer and from the laboratory coating system to the viscometer, all of which we need for the continuous further development of our products and technologies. Our goal is to help you find the best possible packaging solution for your medical devices. Our services range from application-oriented consulting, to the production of high-quality packaging and to the implementation in your packaging process.
Production - Made in Germany
Our products are manufactured on state-of-the-art printing and coating systems as well as cutting and finishing machines under clean room conditions (class ISO 8 according to DIN EN ISO 14644 part 1 and 3). This is done on the basis of carefully validated production processes. These include around the clock in-process controls and complete IT-based traceability of all materials used. We test our products with up-to-date laboratory technology and analytics, thus ensuring the highest product quality. With the system certification ISO 13485 granted, VP Medical Packaging’s clean room production manufacturing standards have been certified proving that we meet today’s demands. As a VP customer, you can rely on our medical packaging at any time.
Safety and quality
The requirements of national and international standards and laws for medical devices form the basis for the development and manufacturing of our products. We not only check the strict compliance with the standard requirements on our own responsibility, but also have us checked by independent renowned external bodies. For example, our sterile barrier systems and packaging materials for medical devices are regularly tested by accredited bodies for compliance with the requirements of the ISO 11607 and EN 868 standards. These regular and documented tests are an important proof of the safety and quality that we provide to our customers and which our customers can claim for their own medical devices.
Service and advice
With our application technology, we offer our customers a highly appreciated additional value. With a short reaction time, we are pleased to come to you and solve the problems together on site. Regular training of our employees is the basis for the fact that we are always able to handle the most modern packaging processes in your plant, be it the packaging process itself or the periphery of your process, such as inline printing or your labelling systems. Our application technology derives directly from our development department and we thus live a seamless transfer of knowledge directly into our development processes. Together with our customers, we are constantly learning and improving gently but consistently. We act in complete agreement with our customers and with the comprehension of the special requirements for validation and documentation of the processes. By confidential exchange of information, we bring you into the ideal starting position for an uncomplicated and successful fulfilment of all regulatory obligations.
Our wide assortment includes paper, non-woven material and DuPont™ Tyvek® for flat packaging (4SS) and form fill seal packaging (FSS) as rollstock, pouches and reels as well as holistic system solutions. Our aim is to continuously develop our products based on your requirements and valid standards and laws for medical devices.
Environmentally conscious action is part of our corporate policy: We work 100% climate neutral. Unavoidable emissions are fully compensated by internationally recognised emission reduction certificates. In addition, we meet all the requirements of DIN EN ISO 14001 for environmental management and ISO 50001 for energy management.