The FDA QSR and the Medical Device Directive specify certain records that should be included in your organization's quality system - Design History File (DHF), Device Master Record (DMR), Device History Record (DHR), and Technical File (TF). Price: $245.00USAGlobalCompliancePanel,Livermore Common, Fremont, CA, 94539USA Phone:800-447-9407Fax: 302-288-6884
When
11 Apr 2013 @ 10:00 am
11 Apr 2013 @ 11:00 am
Duration: 1 hours
Timezone: GMT -8:00
Where
Online Webinar
Language
English en
Organised by
GlobalCompliancePanel (deactivated)Speakers
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