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DTSTART:19700308T020000
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UID:2140535:Event:72803
DTSTAMP:20260531T062012Z
SUMMARY:Expectations of Regulatory & Validation Master Planning - 2017
DESCRIPTION:Overview:  This presentation will cover the importance of
  master planning. The FDA and other regulatory bodies expect these to 
 be among the Quality System documentation.Areas Covered in the Session
 :History and backgroundTypesOrganizationRequirementsRegulatory expecta
 tionsMaintenanceWho Will Benefit:Compliance PersonnelQA Personnelvalid
 ation PersonnelSpeaker Profile: Louis Angelucci is a pharmaceutical pr
 ofessional and Certified Quality Engineer with over 20 years of experi
 ence in Quality Assurance, Quality Control, Validation, consent decree
  remediation as well as cGMP Compliance in the Medical Device and Phar
 maceutical industries.Contact Detail:Compliance4All DBA NetZealous,Pho
 ne: +1-800-447-9407Email: support@compliance4All.com\n\nFor more infor
 mation visit https://medtechiq.ning.com/events/expectations-of-regulat
 ory-validation-master-planning-2017
DTSTART;TZID=America/New_York:20170720T100000
DTEND;TZID=America/New_York:20170720T110000
CATEGORIES:webinar
LOCATION:Online
WEBSITE:http://www.compliance4all.com/control/w_product/~product_id=50
 1357LIVE?channel=medtechiq.ning_Jul_2017_SEO
URL:http://www.compliance4all.com/control/w_product/~product_id=501357
 LIVE?channel=medtechiq.ning_Jul_2017_SEO
CONTACT:18004479407
ORGANIZER:Netzealous LLC DBA - Compliance4All
ATTACH;FMTTYPE="image/jpeg":http://storage.ning.com/topology/rest/1.0/
 file/get/2562014389?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN="Adam Fle
 ming":https://medtechiq.ning.com/profile/Compliance4all
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