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:68436
DTSTAMP:20260412T063253Z
SUMMARY:Webinar on Effective Internal Audit Program
DESCRIPTION:Description :\n\"Internal Audit is a required part of an e
 ffective quality system. More importantly, it is an incredibly powerfu
 l tool to identify areas of non-compliance. A well designed audit prog
 ram can be an effective tool in understanding, communicating, and redu
 cing compliance risk.\nHowever, estimates indicate that up to 75% of c
 ompanies conduct audits only because they are required to by regulatio
 n. Businesses often see internal audit as a non-value added activity l
 eading to meaningless findings, bureaucracy, and cumbersome processes.
  In spite of having an internal audit program, management is often sur
 prised when they receive a 483, Warning Letter, or even a Consent Decr
 ee.\nWithout an effective audit program, management is blind to many o
 f the risks they face in delivering quality medical devices to their c
 ustomers. We will discuss red-flags that indicate your audit and corre
 ctive action systems are not effectively and efficiently identifying a
 nd mitigating compliance risk. We will cover how to make your audit pr
 ogram meaningful and a key tool in maintaining and improving your Qual
 ity System.\"\nMany companies are surprised when they get a 483 or War
 ning Letter. They have been blind to compliance risks within their own
  organization. This webinar can help you understand how to use Interna
 l Audit as a powerful tool to understand, communicate, and mitigate co
 mpliance and quality issues. You will learn how to effectively and eff
 iciently develop your audit program and reduce your quality and compli
 ance risks. You will discover some of the \"red flags\" that indicate 
 your company is taking unacceptable risks.\nAreas Covered in the Sessi
 on :\nRisk Assessment\nDeveloping a Structured Program\nHow to develop
  an Audit Hierarchy\nEnsure Your Audit Staff is Well Trained to Proact
 ively Identify, Communicate, Escalate Issues\nCulture of Quality\nPrio
 ritize, Resources, and Implement Corrective Actions\nMonitoring and Co
 mmunicating Risk\nResidual Risk\nRed Flags\nWho Will Benefit:\nComplia
 nce Managers\nQuality Managers\nCompliance Directors\nQuality Director
 s\nRegulatory AffairsProfessionals\nAuditors\nCompliance Specialists\n
 Professionals performing due diligence and management review\nFor more
  information and enquiries contact us at\nCompliance Trainings\n5939 C
 andlebrook Ct, Mississauga, ON L5V 2V5, Canada  Customer Support : 
 #416-915-4458  Email : support@compliancetrainings.com\nFor more inf
 ormation about this event please visit\nhttps://compliancetrainings.co
 m/SiteEngine/ProductDetailView.aspx?id=MD1634\n\nFor more information 
 visit https://medtechiq.ning.com/events/webinar-on-effective-internal-
 audit-program
DTSTART;TZID=America/New_York:20160310T130000
DTEND;TZID=America/New_York:20160310T140000
CATEGORIES:webinar
LOCATION:Online
WEBSITE:https://compliancetrainings.com/SiteEngine/ProductDetailView.a
 spx?id=MD1634
URL:https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?
 id=MD1634
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
END:VEVENT
END:VCALENDAR