Phone: 800-447-9407
RAPS Approved Webinar on
Design History File (DHF), Device Master Record (DMR), Device History
Record (DHR) and Technical File (TF) - Regulatory Documents
Explained
Date: Thursday, November 8, 2012 Time: 10:00 AM PDT | 01:00 PM EDT...
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Phone: 800-447-9407
RAPS Approved Webinar on
Design History File (DHF), Device Master Record (DMR), Device History
Record (DHR) and Technical File (TF) - Regulatory Documents
Explained
Date: Thursday, November 8, 2012 Time: 10:00 AM PDT | 01:00 PM EDT
Course "Design History File (DHF), Device Master
Record (DMR), Device History Record (DHR) and
Technical File (TF) - Regulatory Documents
Explained" has been pre-approved by RAPS as
eligible for up to 1.
00 credits towards a participant s
RAC recertification upon full completion.
Duration: 60 Minutes
Instructor: Jeff Kasoff
Location: Online
Price : $245.
00 (for one participant)
Jeff Kasoff
Director of Regulatory
Affairs, Life-Tech, Inc
Register Now
Jeff Kasoff, RAC, is the Director of Quality at Byrne Medical, a leading manufacturer of endoscopy and
colonoscopy devices, where he oversees the operation of the quality system.
In this position, .
.
.
more
Overview:
The FDA QSR and the Medical Device Directive specify certain documents or
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