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:79727
DTSTAMP:20260530T144115Z
SUMMARY:Quality Agreements Made Easy (Advanced 2018)
DESCRIPTION:Overview:The requirements for the assurance of quality wit
 hin networks and circles of entities whose responsibilities are increa
 sing specialized present an especially vexing challenge to the managem
 ents of each of these organizations. The specification developer must 
 be aware of the capabilities of the contract manufacturer and the cont
 ract manufacturer must be aware of the limitations of the specificatio
 n developer, for example.\nWhy should you Attend:To the extent that an
 yone responsible within a specification developer, contract design org
 anization, purchasing organization, supplier of critical or crucial ma
 terials or services, or contract manufacturing and/or testing organiza
 tion is concerned about conformity to the ISO 13485:2016 or compliance
  to the FDA regulations and imminent European Medical Device Regulatio
 n, this webinar is for you.\nAreas Covered in the Session:What are the
  consequences of mistakes in quality agreements?How hard does drafting
  a meaningful quality agreement have to be?What do regulators look for
  in these quality agreements?How often should a quality agreement be r
 eviewed? Revised?What if I cannot achieve agreement with the other par
 ty?Tips for making a quality agreement acceptable to all\nWho Will Ben
 efit:Regulatory ManagementRegulatory ConsultantsQuality ManagementSale
 s & Marketing ManagementScientific Staff (Advisors)Clinical Staff (Adv
 isors)Research & Development Management\nSpeaker Profile:Shep Bentley 
 is the President and Principal Consultant for Bentley Biomedical Consu
 lting, LLC, where he is responsible for regulatory strategies leading 
 to FDA approvals and clearances for digital medical device companies. 
 Shep began his career in 1984 at the Hospital Corporation of America a
 s a research technician, and worked at McGaw Labs in Irvine, responsib
 le for GMPs until 1989, when he joined TOSHIBA America where he manage
 d production of various digital devices.\nEvent Fee: One Dial-in One A
 ttendee Price: US$150.00\nContact Detail:Compliance4All DBA NetZealous
 ,Phone: +1-800-447-9407Email: support@compliance4All.com\n\nFor more i
 nformation visit https://medtechiq.ning.com/events/quality-agreements-
 made-easy-advanced-2018
DTSTART;TZID=America/New_York:20180914T100000
DTEND;TZID=America/New_York:20180914T110000
CATEGORIES:webinar
LOCATION:Online
WEBSITE:http://www.compliance4all.com/control/w_product/~product_id=50
 2081LIVE?channel=medtechiq_Sep_2018_SEO
URL:http://www.compliance4all.com/control/w_product/~product_id=502081
 LIVE?channel=medtechiq_Sep_2018_SEO
CONTACT:8004479407
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/2562031566?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN="Adam Fle
 ming":https://medtechiq.ning.com/profile/Compliance4all
END:VEVENT
END:VCALENDAR
