Successful recertification according to ISO (GMP)
In 2019, Sensoplast once again successfully met the requirements of the relevant standards (BS EN ISO 9001, BS EN ISO 15378 and parts of BS EN ISO 13485 as well as the Medical Device Directive 93/42/EEC MMD).
In January, our certifier, TÜV Rheinland, confirmed for the tenth year in succession that we have implemented all organisational and hygienic requirements of these stringent specifications in line with the standards after an on-site audit lasting several days.
We are very proud that the cleanliness of all production areas and the frankness of the interviewed subjects (i.e. all our colleagues) was particularly emphasised. Once again, our production conditions and highly automated processes lived up to the standards of the best in the industry in an international comparison. However, we don't want to simply rest on our laurels. Sensoplast works continuously to meet the latest guidelines for the production of pharmaceutical primary packaging and medical products and to fulfil the standard requirements.