Positive ISO 13485:2003 certification renewal audit for Creaspine®
Creaspine® SAS, is pleased to announce that it has successfully completed the renewal audit ISO 13485:2003 certification for medical device quality management.
In 2007, Creaspine had been granted the ISO 13485:2003 certification of its quality system. Three years later, the renewal audit has been conducted according to the new European Directive 2007/47/EC.
“Leveraging its past success from last summer with FDA audit, Creaspine confirms its performance with the achievement of this ISO renewal audit. They both validate our strong commitment to delivering the highest quality service and satisfaction that our customers have come to expect. I am proud of the organisation and confident in its ability to deliver more High Quality Innovative products” said Philippe Jenny MD, President of Creaspine SAS.
The auditor particularly emphasized the willingness and ability of the entire team to meet the requirements, to provide high quality documentation and to present a complete, thorough and meaningful post-marketing data report on the products already on the markets.
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