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UID:2140535:Event:65641
DTSTAMP:20260524T032621Z
SUMMARY:Webinar on Implementing an Internal Audit Program of QMA, Pers
 isting to ISO 13485 and 21 CFR Part 820
DESCRIPTION:Description :\nThis webinar is intended to help you adequa
 tely develop an internal audit program of a firm's quality management 
 system (QMS) as required by ISO 13485 or 21 CFR Part 820.\n21 CFR 820.
 22 states \"Each manufacturer shall establish procedures for quality a
 udits and conduct such audits to assure that the quality system is in 
 compliance with the established quality system requirements and to det
 ermine the effectiveness of the quality system.\"\nThis webinar will p
 rovide great opportunities to help you adequately establish your inter
 nal quality audit program with increased awareness and familiarity by 
 employing risk- and process-based approaches pursuant to both ISO 1348
 5 and 21 CFR 820.22.\nAt the end of the webinar, you will become famil
 iar with the regulatory requirements for establishing an adequate inte
 rnal audit program while bringing great benefits and added values to y
 our firm's quality management system and contributing to saving an eno
 rmous amount of resources.\nThis webinar is a must to attend to ensure
  the adequacy of your internal audit program in conformity with the re
 quirements set out in the ISO 13485 and 21 CFR 820.22.\nAreas Covered 
 in the Session :\nStatutes and Regulations\nDefinitions\nComparative O
 verview of both ISO 13485 and 21 CFR Part 820\nAuditing Strategy\nAudi
 t Objectives\nAudit Planning, Frequency, Duration and Logistics\nHow t
 o Audit Quality Management Systems\nVarious Audit Approaches\nQuality 
 Systems and Subsystems in ISO 13485\nQuality Systems and Subsystems un
 der 21 CFR Part 820\nFDA and ISO 13485\nGood Practices: Speaker’s Su
 ggestions and Recommendations\nConclusion\nWho Will Benefit:\nQuality 
 Professionals\nCompliance Staff and Officers\nRegulatory Affairs\nRese
 arch & Development\nChief Executive Officers\nVice Presidents\nAttorne
 ys\nClinical Affairs\nConsultants\nContractors/Subcontractors\nAnyone 
 Interested in the Topic for ISO 13485 or 21 CFR Part 820\nPrice tags:\
 nLive\nSingle Live : For One Participant\n$ 249\nCorporate Live : For 
 Max. 10 Participants\n$ 899\nRecording\nSingle REC : For One Participa
 nt - Unlimited Access for 6 Months\n$ 299\nFor more information and en
 quiries contact us at\nCompliance Trainings\n5939 Candlebrook Ct, Miss
 issauga, ON L5V 2V5, Canada\nCustomer Support : #416-915-4458\nEmail :
  support@compliancetrainings.com\nFor more information about this even
 t please visit\nhttps://compliancetrainings.com/SiteEngine/ProductDeta
 ilView.aspx?id=MD1510\nLike Us On Facebook:\nhttps://www.facebook.com/
 events/580355818766626/?source=1&sid_create=1108234639\n\nFor more inf
 ormation visit https://medtechiq.ning.com/events/webinar-on-implementi
 ng-an-internal-audit-program-of-qma
DTSTART;TZID=America/New_York:20151002T130000
DTEND;TZID=America/New_York:20151002T140000
CATEGORIES:webinar
LOCATION:Online
WEBSITE:https://compliancetrainings.com/SiteEngine/ProductDetailView.a
 spx?id=MD1510
URL:https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?
 id=MD1510
CONTACT:4169154458
ORGANIZER;CN=compliancetrainings:https://medtechiq.ning.com/profile/co
 mpliancetrainings
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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