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DTSTAMP:20260526T042054Z
SUMMARY:6-Hour Virtual Seminar on Medical Device Single Audit Program
DESCRIPTION:Global Medical Device Regulations continue to evolve, as d
 evices become more diverse and sophisticated. Understanding the regula
 tions and requirements in your targeted markets will expedite speed-to
 -market of innovative products and assist patients needing access to l
 ife-saving  products and technologies. Government Regulatory Authorit
 ies, needing to become more efficient with their time, are looking for
  ways to better use their internal resources without compromising safe
 ty in products, which become marketable.\nOne such example is the Medi
 cal Device Single Audit Program [MDSAP], where Authorized Organization
 s would be allowed to carry out a single GMP audit on medical device m
 anufacturing facilities and have it stand to support registrations acr
 oss the current participating member countries: U.S. Canada, Brazil, A
 ustralia and Japan. Health Canada has now made the MDSAP process manda
 tory for all licensed products in Canada.\nhttps://www.globalcomplianc
 epanel.com/virtual-seminar/-10423LIVE?channel=medtechiq-May_2020_SEO\n
 \nFor more information visit https://medtechiq.ning.com/events/6-hour-
 virtual-seminar-on-medical-device-single-audit-program
DTSTART;TZID=America/New_York:20200513T080000
DTEND;TZID=America/New_York:20200513T140000
CATEGORIES:webinar
LOCATION:Online Event
WEBSITE:https://www.globalcompliancepanel.com/virtual-seminar/-10423LI
 VE?channel=medtechiq-May_2020_SEO
URL:https://www.globalcompliancepanel.com/virtual-seminar/-10423LIVE?c
 hannel=medtechiq-May_2020_SEO
CONTACT:8004479407
ORGANIZER;CN="John Robinson":https://medtechiq.ning.com/profile/JohnRo
 binson
ATTACH;FMTTYPE="image/jpeg":https://storage.ning.com/topology/rest/1.0
 /file/get/3768168694?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN="John Rob
 inson":https://medtechiq.ning.com/profile/JohnRobinson
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