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DTSTART:19700308T020000
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UID:2140535:Event:472104
DTSTAMP:20260521T104554Z
SUMMARY:SOP Writing, Training and Compliance in the Pharmaceutical Ind
 ustry
DESCRIPTION:Standard Operating Procedures (SOPs) are the basis for a l
 arge part of the day-to-day training that most pharmaceutical employee
 s are required to perform. Still, it is not widely understood the exte
 nt of the commitments we make when we write an SOP or how the writing 
 of the SOP can have a positive or negative impact on training or job p
 erformance. For example, there is an expectation that procedures descr
 ibe the most critical processes for product manufacturing and will be 
 followed consistently, with few if any deviations. In this course you 
 will learn the keys to writing effective SOPs, the vital connection be
 tween the documentation and training spheres, and how to maximize this
  connection to improve the quality of both SOPs and training.\nTo acco
 mplish these goals, we will review regulatory agency expectations when
  an SOP is written, provide suggestions for uncovering the process in 
 its entirety and describe it clearly and concisely, indicate how to br
 eak portions of the process(es) into logical chunks, and show how the 
 SOP and the training program can work together harmoniously.\n\nUnders
 tanding how the average employee is swamped with more work than they c
 an manage, we will also provide tips for shortening this process and t
 ake advantage of tools that probably already exist in the systems that
  you use on a day-to-day basis. We will provide valuable insights and 
 examples that reflect the extensive experience of the instructor in th
 e documentation and training fields., and which can assist you in writ
 ing and implementing SOPs with maximum efficiency and effectiveness.\n
 \nLearning Objectives:\n\nTo improve the writing of SOPs for more effe
 ctive training and reduction of errors.\nTo understand the regulatory 
 implications of what is written in an SOP\nTo learn the parameters of 
 an effective SOP\nTo distinguish a well-written SOP from a poorly writ
 ten one\nTo define processes better by effective interaction with the 
 SOP process owner and/or author\nTo integrate the SOP effectively into
  the position curricula of employees\nTo explore the connection betwee
 n SOPs and job performance, and measure retention of SOP content at th
 e training stage\n\n\nAreas Covered :\n\nRegulatory requirements for S
 OPs\nUsing process excellence tools to create a robust process and pro
 cedure\nWhat commitments you make when you put your process in writing
 \nKeeping training in mind while writing procedures\nConsequences of n
 oncompliance\n\n\n\nWho will Benefit:\nPharmaceutical industry, partic
 ularly those areas that develop SOPs for the manufacturing or quality 
 monitoring of pharmaceutical products, as well as Information Technolo
 gy (IT)\n\nFor more information visit https://medtechiq.ning.com/event
 s/sop-writing-training-and-compliance-in-the-pharmaceutical-2
DTSTART;TZID=America/New_York:20220418T100000
DTEND;TZID=America/New_York:20220419T170000
CATEGORIES:seminae
LOCATION:online
WEBSITE:https://www.complianceonline.com/sop-writing-in-pharma-gmp-env
 ironment-seminar-training-80560SEM-prdsm?channel=MedTech%20I.Q
URL:https://www.complianceonline.com/sop-writing-in-pharma-gmp-environ
 ment-seminar-training-80560SEM-prdsm?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/10168482492?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN=Complianc
 eOnline:https://medtechiq.ning.com/profile/Referral512
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