Sealed Air Nelipak® is certified to EN ISO 13485: 2003 and EN ISO 9001: 2008.
Certificate expiry date: August 1, 2012.
At all levels of the organisation, Nelipak® continuously improves its procedures and processes. All our employees are responsible for monitoring and improving the quality of their work. The production operations for medical and pharmaceutical products are based on the GMP guidelines.
Additionally, Nelipak® has a thorough product traceability system. The raw materials, auxiliary materials, inspection results, production conditions and person responsible can be traced for all our products, up to six years after the date of manufacturing.
Process control
The operators take measurements at set times, using an automated statistical process control (SPC) system. This ensures that the process performance is continuously monitored and that any process upsets are detected at an early stage. Of course, quality plans are available for all products, setting out the quality criteria and process stages.
Receiving inspection
Sealed Air Nelipak® purchases raw and auxiliary materials from carefully selected suppliers. Where necessary, the critical properties of these materials are verified.
Complaints procedure
Nelipak® takes any complaints seriously. Complaints are entered into an automated system. The affected departments investigate the issue and then take corrective and preventive action. The quality department coordinates the procedure and complaints are monitored continuously. We analyse the type of complaint, what caused it, the department responsible and how serious it is. Nelipak® uses these analyses to plan long-term improvement measures.
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