BEGIN:VCALENDAR
PRODID:NingEventWidget-v1
VERSION:2.0
METHOD:PUBLISH
BEGIN:VTIMEZONE
TZID:America/New_York
X-LIC-LOCATION:America/New_York
BEGIN:DAYLIGHT
TZOFFSETFROM:-0500
TZOFFSETTO:-0400
TZNAME:EDT
DTSTART:19700308T020000
RRULE:FREQ=YEARLY;BYMONTH=3;BYDAY=2SU
END:DAYLIGHT
BEGIN:STANDARD
TZOFFSETFROM:-0400
TZOFFSETTO:-0500
TZNAME:EST
DTSTART:19701101T020000
RRULE:FREQ=YEARLY;BYMONTH=11;BYDAY=1SU
END:STANDARD
END:VTIMEZONE
BEGIN:VEVENT
UID:2140535:Event:78297
DTSTAMP:20260523T121029Z
SUMMARY:Medical Device Single Audit Program Preparation
DESCRIPTION:Overview:The International Medical Device Regulators Forum
  (IMDRF) recognizes that a global approach to auditing and monitoring 
 the manufacturing of medical devices could improve their safety and ov
 ersight on an international scale.\nWhy should you Attend:Today with a
  single audit, it is possible for a medical device manufacturer to sat
 isfy the quality management system requirements of Australia, Brazil, 
 Canada, Japan and the USA! This is the benefit of the Medical Device S
 ingle Audit Program, or MDSAP. However, there are some vital considera
 tions before embarking upon this approach to satisfying the regulators
  of five major markets.\nAreas Covered in the Session:Origin of MDSAPA
 pplicability of MDSAPAdvantages of MDSAPDisadvantages of MDSAP\nWho Wi
 ll Benefit:Corporate Management (Presidents, CEOs, COOs)Quality Manage
 ment (Vice Presidents, Directors, Managers)Regulatory Management (Vice
  Presidents, Directors, Managers)Sales & Marketing Management (Vice Pr
 esidents, Directors, Managers)\nSpeaker Profile:Shep Bentley is the Pr
 esident and Principal Consultant for Bentley Biomedical Consulting, LL
 C, where he is responsible for regulatory strategies leading to FDA ap
 provals and clearances for digital medical device companies. Shep bega
 n his career in 1984 at the Hospital Corporation of America as a resea
 rch technician, and worked at McGaw Labs in Irvine, responsible for GM
 Ps until 1989, when he joined TOSHIBA America where he managed product
 ion of various digital devices.\nEvent Fee: One Dial-in One Attendee P
 rice: US$150.00\nContact Detail:Compliance4All DBA NetZealous,Phone: +
 1-800-447-9407Email: support@compliance4All.com\n\nFor more informatio
 n visit https://medtechiq.ning.com/events/medical-device-single-audit-
 program-preparation
DTSTART;TZID=America/New_York:20180406T100000
DTEND;TZID=America/New_York:20180406T110000
CATEGORIES:online
LOCATION:Online
WEBSITE:http://www.compliance4all.com/control/w_product/~product_id=50
 1820LIVE?channel=medtechiq_Apr_2018_SEO
URL:http://www.compliance4all.com/control/w_product/~product_id=501820
 LIVE?channel=medtechiq_Apr_2018_SEO
CONTACT:18004479407
ORGANIZER;CN="Adam Fleming":https://medtechiq.ning.com/profile/Complia
 nce4all
ATTACH;FMTTYPE="image/jpeg":http://storage.ning.com/topology/rest/1.0/
 file/get/2562015937?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN="Adam Fle
 ming":https://medtechiq.ning.com/profile/Compliance4all
END:VEVENT
END:VCALENDAR
