BEGIN:VCALENDAR
VERSION:2.0
PRODID:-//Clinical Trial Events//Event calendar//EN
CALSCALE:GREGORIAN
METHOD:PUBLISH
BEGIN:VEVENT
UID:qt7ic9j8i@clinicaltrialevents.com
DTSTAMP:20261104T144819Z
DTSTART:20261202T170000Z
DTEND:20261202T180000Z
SUMMARY:ACRP Webinar: ICH E6(R3) Explained: From Regulatory Principles to C
 linical Trial Practice
DESCRIPTION:https://clinicaltrialevents.com/events/acrp-webinar-ich-e6r3-ex
 plained-from-regulatory-principles-to-clinical-trial-practice-qt7ic9j8i\n\
 nA free live ACRP webinar giving an overview of ICH E6(R3): the rationale 
 for the revision\, its core principles\, and key changes such as Quality b
 y Design\, risk-proportionate approaches\, data governance\, computerized 
 systems\, and essential records. It then covers what the guideline means i
 n practice for document management\, sponsor-site collaboration\, and insp
 ection readiness. Sponsored by Agatha Inc.\; no ACRP contact hours.
LOCATION:https://clinicaltrialevents.com/events/acrp-webinar-ich-e6r3-expla
 ined-from-regulatory-principles-to-clinical-trial-practice-qt7ic9j8i
URL:https://clinicaltrialevents.com/events/acrp-webinar-ich-e6r3-explained-
 from-regulatory-principles-to-clinical-trial-practice-qt7ic9j8i
STATUS:CONFIRMED
END:VEVENT
END:VCALENDAR