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:65058
DTSTAMP:20260524T121552Z
SUMMARY:Webinar On Good Laboratory Practice Regulations - Introduction
  and Strategies for Implementation
DESCRIPTION:Description :\nComplying with GLP regulations can increase
  the cost of a laboratory up to 30%. Companies or employees either don
 't know exactly what GLP really means, or what procedures are required
  and how to implement GLP regulations. Lack of GLP knowledge is also a
 n inspection issue as training plans should include basic GLP knowledg
 e for everybody working in a GLP environment. Attend the seminar to ge
 t a good understanding on GLP regulations and get best practice guides
  and strategies for easy implementation.\nAreas Covered in the Session
  :\nFDA and International GLP regulations: 21 CFR Part 58, OECD\nExamp
 les for FDA 483 inspectional observations and warning letters\nObjecti
 ves, scope and concepts of GLP's\nSpecial organizational requirements\
 nResponsibilities: Management, Study director, QA, analysts\nSOP requi
 rements: type, formats and enforcement\nGLP studies: preparation, cond
 uct, documentation\nKey requirements for equipment, facilities referen
 ce material, people\nData generation and evaluation: raw data, interme
 diate results, final results\nRecords keeping: format, length of time,
  archiving and reprocessing\nStrategies for Multi-site GLP Studies\nPr
 eparing for FDA inspections\nWho Will Benefit:\nEverybody getting invo
 lved in GLP studies\nLab Supervisors and managers\nQA managers and per
 sonnel\nGLP auditors\nAnalysts\nConsultants\nTeachers\nPrice Tags:\nLi
 ve\nSingle Live : For One Participant\n$ 249\nCorporate Live : For Max
 . 10 Participants\n$ 899\nRecording\nSingle REC : For One Participant 
 - Unlimited Access for 6 Months\n$ 299\nFor more information and enqui
 ries contact us at\nCompliance Trainings\n5939 Candlebrook Ct, Missis
 sauga, ON L5V 2V5, Canada Customer Support : 4169154458  Email : su
 pport@compliancetrainings.com\nFor more information about this event p
 lease visit\nhttps://compliancetrainings.com/SiteEngine/ProductDetailV
 iew.aspx?id=FDB1451\nhttps://www.facebook.com/events/1524037371203508/
 ?source=1&sid_create=3132374451\n\nFor more information visit https://
 medtechiq.ning.com/events/webinar-on-good-laboratory-practice-regulati
 ons-introduction-and
DTSTART;TZID=America/New_York:20150219T130000
DTEND;TZID=America/New_York:20150219T141500
CATEGORIES:webinar
LOCATION:Online
WEBSITE:https://compliancetrainings.com/SiteEngine/ProductDetailView.a
 spx?id=FDB1451
URL:https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?
 id=FDB1451
CONTACT:4169154458
ORGANIZER:complianceTrainings
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
