isocertificate90012008-CertificateofRegistration.PDFVIP

isocertificate90012008-CertificateofRegistration.PDF

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isocertificate90012008-CertificateofRegistration

Certificate of Registration QUALITY MANAGEMENT SYSTEM - ISO 13485:2003 EN ISO 13485:2012 This is to certify that: Life Technologies AS Ullernchausseen 52 Oslo 0379 Norway Holds Certificate Number: MD 567972 and operates a Quality Management System which complies with the requirements of ISO 13485:2003 EN ISO 13485:2012 for the following scope: Design, development, manufacturing, and sales of products either used as standalone in-vitro diagnostic (IVD) products, or for further manufacturing of OEM products for IVD markets. Design, development, manufacturing, and sales of products intended for ex-vivo separation of human cells, and for cell-based clinical research. For and on behalf of BSI: Frank Lee, EMEA Compliance Risk Director Original Registration Date: 19/11/2010 Effective Date: 16/10/2015 Latest Revision Date: 14/10/2015 Expiry Date: 15/10/2018 Page: 1 of 2 This certificate was issued electronically and remains the property of BSI and is bound by the conditions of contract. An electronic certificate can be authenticated online. Printed copies can be validated at /ClientDirectory Information and Contact: BSI, Kitemark Court, Davy Avenue, Knowlhill, Milton Keynes MK5 8PP. Tel: + 44 845 080 9000 BSI Assurance UK Limited, registered in England under number 7805321 at 389 Chiswick High Road, London W4 4AL, UK. A Member of the BSI Group of Companies. Life Technologies AS Ullernchausseen 52 Oslo 0379 Norway Design, development, manufacturing, and sales of products either used as standalone in-vitro diagnostic (IVD) products, or for further manufacturing of OEM products for IVD markets. Design, development, manufacturing, and sales of products intended for ex-vivo separation of human cells, and for cell- based clinical research. Life Technologies AS Svelleveien 29 Lillestrom 2001 Norway Design, development, manufacturing, and sales of products either used as standalone in-vitro diagnostic (IVD) products, or for further manufacturing of OEM products for IVD markets.

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