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:64988
DTSTAMP:20260405T151330Z
SUMMARY:Webinar On How to Develop a Master Validation Plan
DESCRIPTION:Every medical device company (OEM) must meet certain stand
 ards for validation of its transfer plans, facilities, clean rooms and
  processes. These standards apply for OEM’s and suppliers to OEM’s
 . Many medical companies have never had a Master Validation Plan for t
 heir facilities, processes or suppliers. This is an important standard
  to have when being audited to show on big picture compliance to FDA a
 nd foreign standards.\nThis webinar on “How to Develop a Master Vali
 dation Plan” (also known as Validation Master Plan) will provide a s
 tep-by-step procedure for all medical device companies and their suppl
 iers that are in need of developing a plan for product/equipment trans
 fer, facilities, processes or to develop a company standard.\nAreas Co
 vered in the Session :\nMaster Validation Plan content\nRevision histo
 ry\nBackground\nObjective\nPurpose\nScope\nProject approach\nKey activ
 ities\nProject organization\nCommunication plan\nQuality Assurance\nFa
 cility approach\nValidation approach\nSchedule\nBudget ...and more\nWh
 o Will Benefit:\nOEM Senior management\nSupplier Senior management\nMa
 nagers and directors\nManagers setting up new facilities and product l
 ines\nPlant and facility managers\nEnd-users responsible for design co
 ntrol and product development\nR&D and product development\nProject ma
 nagers\nFacility and clean room designers\nProcess engineers and manag
 ers\nValidation engineers\nQuality management and engineers\nAuditors\
 nSuppliers to medical OEM’s\nConsultants\nPrice Tags:\nLive\nSingle 
 Live : For One Participant\n$ 249\nCorporate Live : For Max. 10 Partic
 ipants\n$ 899\nRecording\nSingle REC : For One Participant - Unlimited
  Access for 6 Months\n$ 299\nFor more information and enquiries contac
 t us at\nCompliance Trainings\n5939 Candlebrook Ct, Mississauga, ON L
 5V 2V5, Canada  Customer Support : #416-915-4458  Email : support@
 compliancetrainings.com\nFor more information about this event please 
 visit\nhttps://compliancetrainings.com/SiteEngine/ProductDetailView.as
 px?id=MD1186\n\nFor more information visit https://medtechiq.ning.com/
 events/webinar-on-how-to-develop-a-master-validation-plan
DTSTART;TZID=America/New_York:20150127T130000
DTEND;TZID=America/New_York:20150127T140000
CATEGORIES:webinar
LOCATION:Online
WEBSITE:https://compliancetrainings.com/SiteEngine/ProductDetailView.a
 spx?id=MD1186
URL:https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?
 id=MD1186
CONTACT:4169154458
ORGANIZER:Compliance Trainings
ATTACH;FMTTYPE="image/jpeg":
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN=complianc
 etrainings:https://medtechiq.ning.com/profile/compliancetrainings
END:VEVENT
END:VCALENDAR