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UID:2140535:Event:64977
DTSTAMP:20260524T103724Z
SUMMARY:Webinar On Key Factors to Write an Effective Standard Operatin
 g Procedure (SOP) and Work Instructions (WIs)
DESCRIPTION:This webinar will instruct the participant on how to write
 , organize, and maintain SOPs and train personnel in a way that will e
 nsure compliance in a way that is concise, reproducible and easy to fo
 llow. It will begin with a strategic view of SOPs in a company and how
  SOPs can help streamline operations in addition to ensuring regulator
 y compliance. This will be followed by explanation on how to get from 
 regulations to the SOP. Finally, Best Practices for creating, implemen
 ting and maintaining SOPs using a risk based approach and getting SOPs
  ready for inspection will be presented.\nVirtually every FDA inspecti
 on includes a review of SOPs and adverse agency findings are often the
  result of SOP administration issues.\nStandard Operating Procedures (
 SOPs) are required by law for companies that are regulated by the Code
  of Federal Regulations such as Title 21 and Title 493. Yet there is n
 o guidance on how to write, organize and maintain SOPs. Consequently, 
 SOPs are frequently written in a way that makes compliance difficult o
 r downright impossible. Worse, this often leads to many regulatory err
 ors that first come to light during a FDA audit.\n \nThis webinar wil
 l show you how to write, organize, and maintain SOPs and train personn
 el in a way that will ensure compliance in a way that is concise, repr
 oducible and easy to follow.\nAreas Covered in the Session :\nSOPs and
  their relation to the regulations\nSOPs as part of the company's regu
 latory infrastructure\nSOP on SOPs and how to ensure conciseness, cons
 istency and ease of use\nRisk Based approach on SOP Best Practices for
  creation and maintenance\nTraining on SOPs\nTools for SOP tracking an
 d when is validation required\nWhat the FDA looks for in SOPs during a
 n inspection\nWho Will Benefit:\nQuality Managers\nQuality Engineers\n
 Small business owners\nGxP\nRegulatory Affairs professionals\nConsulta
 nts\nQuality VPs\nIT VPs\nRegulatory VP\nCEOs\nPrice tags:\nLive\nSing
 le Live : For One Participant\n$ 249\nCorporate Live : For Max. 10 Par
 ticipants\n$ 899\nRecording\nSingle REC : For One Participant - Unlimi
 ted Access for 6 Months\n$ 299\nFor more information and enquiries con
 tact us at\nCompliance Trainings\n5939 Candlebrook Ct, Mississauga, O
 N L5V 2V5, Canada  Customer Support : #416-915-4458  Email : suppo
 rt@compliancetrainings.com\nFor more information about this event plea
 se visit\nhttps://compliancetrainings.com/SiteEngine/ProductDetailView
 .aspx?id=FDB1393\n\nFor more information visit https://medtechiq.ning.
 com/events/webinar-on-key-factors-to-write-an-effective-standard-opera
 ting
DTSTART;TZID=America/New_York:20150113T130000
DTEND;TZID=America/New_York:20150113T143000
CATEGORIES:webinar
LOCATION:Online
WEBSITE:https://compliancetrainings.com/SiteEngine/ProductDetailView.a
 spx?id=FDB1393
URL:https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?
 id=FDB1393
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
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