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Co-ordination of Notified Bodies Medical Devices (NB-MED) on Council Directives 90/385/EEC, 93/42/EEC and 98/79/EC Introduction Issue Page

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Title: Post-Marketing Surveillance (PMS) post …

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NBOG’s Best Practice Guide AIMDD, 2010-3

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Medical Device Directive 93/42/EEC CE-Marking …

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Guidance on Design-Dossier Examination and …

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NBOG’s Best Practice Guide 2009-1 NBOG BPG 2009-1 Page 2 of 6 3.3 The NB should review the manufacturer’s use of harmonised standards. If other standards have been used in place of harmonised standards or where harmonised standards do not

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