BEGIN:VCALENDAR
VERSION:2.0
CALSCALE:GREGORIAN
PRODID:iCalendar-Ruby
BEGIN:VEVENT
LOCATION:The Crowne Plaza Boston-Natick Building Name 
SEQUENCE:0
ORGANIZER:Barnett International
DTEND:20060627T170000
DTSTART:20060626T090000
UID:2009-11-08T18:24:30-05:00_452859490@socialweb1
DTSTAMP:20091108T182430
DESCRIPTION:This course highlights new changes to medical device regulation
 s and provides an overview to the submission of documents to the FDA for ap
 proval of medical device products. Participants gain a better understanding
  of the medical device approval process and the underlying scientific and r
 egulatory principles involved. Guidelines for each aspect of research are p
 rovided\, as well as information on the structuring of submissions and post
 -approval documents. Information on maintaining on-going relationships with
  the FDA is also discussed. The course enables regulatory affairs professio
 nals to provide the FDA with necessary information and obtain product appro
 val.
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SUMMARY:Barnett International: Medical Device Approval Process
LAST-MODIFIED:20060621T140601
CREATED:20060621T140601
END:VEVENT
END:VCALENDAR