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METHOD:PUBLISH
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TZID:America/New_York
X-LIC-LOCATION:America/New_York
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TZOFFSETFROM:-0500
TZOFFSETTO:-0400
TZNAME:EDT
DTSTART:19700308T020000
RRULE:FREQ=YEARLY;BYMONTH=3;BYDAY=2SU
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DTSTART:19701101T020000
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BEGIN:VEVENT
UID:2140535:Event:66321
DTSTAMP:20260522T055313Z
SUMMARY:Webinar On Good Clinical Practices (GCP)
DESCRIPTION:Description :\nThis webinar is intended to help you adequa
 tely implement Good Clinical Practices (GCP) including documentation r
 equirements during clinical trials for both drugs and medical devices.
 \nTo adequately implement GCPs, there are a set of standard operating 
 procedures (SOPs) to be established and maintained at any given facili
 ty, to the extent applicable, as a sponsor, clinical investigators, mo
 nitors, and CROs, etc.\nGCP requirements including documentation requi
 rements (a set of SOPs) with key elements to be contained in the SOP w
 ill be discussed.\nIn this 60-min webinar, you will have unparalleled 
 opportunities to bring great value and benefits to your organization a
 nd to greatly improve your GCPs with increased awareness of the needs 
 - sustainable compliance and patient safety.\nAreas Covered in the Ses
 sion :\nLaws and Regulations\nDefinitions\nClinical Trials and Require
 ments\nRegulatory Requirements for INDs and IDEs.\nDuties and Responsi
 bilities for Clinical Investigators (CI), Institutional Review Boards 
 (IRBs), Sponsors and Monitors, and Contract Research Organizations (CR
 Os)\nICH-GCP Guidelines\nISO 14155\nList of SOPs and Adequate Document
 ation\nKey Elements in the SOPs\nCommon GCP Deficiencies in EU and US\
 nEnforcement Actions\nLessons Learned\nWho Will Benefit:\nClinical Aff
 airs\nRegulatory Affairs\nQuality Assurance\nResearch & Development\nC
 onsultants\nContractors/Subcontractors\nSenior Management\nAnyone Inte
 rested in the Topic\nPrice tags:\nLive\nSingle Live : For One Particip
 ant\n$ 249\nCorporate Live : For Max. 10 Participants\n$ 899\nRecordin
 g\nSingle REC : For One Participant - Unlimited Access for 6 Months\n$
  299\nFor more information and enquiries contact us at\nCompliance Tra
 inings\n5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada  Custo
 mer Support : #416-915-4458  Email : support@compliancetrainings.com
 \nFor more information about this event please visit\nhttps://complian
 cetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1517\n\nFor mo
 re information visit https://medtechiq.ning.com/events/webinar-on-good
 -clinical-practices-gcp
DTSTART;TZID=America/New_York:20150622T130000
DTEND;TZID=America/New_York:20150622T140000
CATEGORIES:webinar
LOCATION:Online
WEBSITE:https://compliancetrainings.com/SiteEngine/ProductDetailView.a
 spx?id=FDB1517
URL:https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?
 id=FDB1517
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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