Quality and hygiene
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It is our policy that all the products and services from Nolato Cerbo must meet the demands and expectations of our customers. We are certified in accordance with ISO 9001 and (as first company in Sweden) ISO 15378. The requirement for Good Manufacturing Practice is being met within our manufacturing procedures. Nolato Cerbo was the first company outside of the United Kingdom to be granted PS 9000 certification.
Production at Nolato Cerbo is carried out under strict observation of hygiene requirements to prevent product contamination. Air cleanliness is controlled on a regular basis and our average air cleanliness is within the specification for ISO class 8 clean zone, according to ISO-14644-1:1999. We operate vision control systems throughout the production process in order to detect any dimensional or visual imperfections.
Documentation pharmaceutical packaging
Nolato Cerbo has full batch documentation where traceability of products and raw material are part of our normal procedures. The batch documentation is retained for 6 years. All our products are listed in a Type III Drug Master File, DMF no 18790.
