Product Labeling

Our Quality Management System

All production-relevant processes at Sensoplast are documented in detail. The existing quality management system is adapted to these processes. The continuous batch tracking of all manufactured components along the complete value chain is ensured. All components as well as the end product are meticulously checked by our quality management team at different stages during the production process. They fulfill the stringent quality standards required of pharmaceutical primary packaging raw materials.

Production, assembly, and packaging take place with low germ content. Sensoplast orientates itself with regards to quality assurance as per the recommendations of the World Health Organization (WHO) to the pharmaceutical industry, of Good Manufacturing Practice (GMP), as well as of the respective valid defect valuation lists for injection molding parts made of plastic: closures, sealing inserts, dosage systems (droppers, etc.), according to publications by the ECV Editio Cantor Verlag für Medizin und Naturwissenschaften GmbH, Aulendorf (German publishing house for medicine and natural science).
Our test results for finished products are regularly documented and are available on request in the form of a comprehensive quality certificate.

SENSOPLAST was successfully certified according to ISO 9001:2008 (Quality Management System) as well as according to ISO 15378:2006* in April 2010.

*Primary packaging materials for medicinal products – Particular requirements for the application of ISO 9001:2000 with reference to Good Manufacturing Practice (GMP)

Our predominantly international customers can be assured at any time of the superior manufacturing, assembly, and packing of primary packaging with attention to process and hygiene-related aspects under controlled quality conditions.

The current certificates (D, E, F) are available for you to download here: