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:468685
DTSTAMP:20260604T205629Z
SUMMARY:Writing and Revising SOPs for Increased Operational Efficiency
DESCRIPTION:This webinar will discuss how to more effectively write an
 d revise standard operating procedures (SOPs) with a focus on increasi
 ng operational efficiencies\nWhy Should You Attend:\n\nAre new staff c
 onfused during training on your SOPs?\nDo you have too many SOPs?\nDo 
 some SOPs give directions that conflict with directions from other SOP
 s?\nAre you writing up deviations far too often?\nDo you have some SOP
 s that just plainly don’t make sense?\n\nThis webinar will highlight
  important fundamental knowledge for writing effectively in the contex
 t of clear, concise, effective SOPs. It will also help focus on an eff
 iciency mindset that can lead to operational gains without sacrificing
  quality.\n.\nAreas Covered in the Webinar:\n\nWhat is an SOP?\nWays t
 o structure systems of SOPs\nExamples of sections to include in an SOP
 \nDo what you say and say what you do\nInternal self-consistency, cons
 istency when referencing other documents\nTips for clear written commu
 nication\nEngaging stakeholders during the process at all levels of th
 e organization\nActively listening\nOrganizational culture’s role in
  success\nSOP authorship, reviewers, and approvers\nTraining on new SO
 Ps and revisions\n\nFrequently Asked Questions:\n\nAre there real worl
 d examples that you have encountered when having a signature block on 
 every SOP page was helpful?\nAre you aware of any FDA observations ass
 ociated with not having signature blocks on every page?\nCan you expla
 in the difference between an SOP and a \"work instruction\" document?\
 nWhat is role of QA in SOP approvals?\n\n\nWho Will Benefit:\n\nProduc
 t Development Managers\nManufacturing Managers\nOperations Directors\n
 R&D Directors\nSafety or EH&S Officers\nRisk Management Officers\nStaf
 f Scientists\nFormulation Scientists\nAnalytical Chemists\nQuality Sys
 tems Director\nQuality Assurance Manager\nQuality Control Supervisor\n
 Laboratory Manager\n\nFrom industries including:\n\nConsumer Goods\nMe
 dical Devices\nDental Products and Devices\nPharmaceuticals\nCosmetics
 \nDietary Supplements\n\n\nFor more information visit https://medtechi
 q.ning.com/events/writing-and-revising-sops-for-increased-operational-
 efficiency-1
DTSTART;TZID=America/New_York:20210720T100000
DTEND;TZID=America/New_York:20210720T130000
CATEGORIES:seminae
LOCATION:online
WEBSITE:https://www.complianceonline.com/writing-revising-sops-operati
 onal-efficiency-webinar-training-706214-prdw?channel=MedTech%20I.Q
URL:https://www.complianceonline.com/writing-revising-sops-operational
 -efficiency-webinar-training-706214-prdw?channel=MedTech%20I.Q
CONTACT:8887172436
ORGANIZER;CN=ComplianceOnline:https://medtechiq.ning.com/profile/Refer
 ral512
ATTACH;FMTTYPE="image/jpeg":https://storage.ning.com/topology/rest/1.0
 /file/get/9025749664?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN=Complianc
 eOnline:https://medtechiq.ning.com/profile/Referral512
END:VEVENT
END:VCALENDAR