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DTSTART:19700308T020000
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UID:2140535:Event:65055
DTSTAMP:20260523T161651Z
SUMMARY:Webinar On Good Documentation Practices for Clinical Trials
DESCRIPTION:Description :\nThis webinar is intended to help you adequa
 tely implement Good Clinical Practices (GCP): in particular, documenta
 tion requirements during clinical trials for both drugs and medical de
 vices.\nTo adequately implement GCPs, there are a set of standard oper
 ating procedures (SOPs) to be established and maintained at any given 
 facility, to the extent applicable, as a sponsor, clinical investigato
 rs, monitors, and CROs, etc.\nThe documentation requirements including
  a set of SOPs with key elements to be contained in the SOP will be di
 scussed.\nIn this 60-min webinar, you will have unparalleled opportuni
 ties to bring great value and benefits to your organization and to gre
 atly improve your GCPs with increased awareness of the needs - sustain
 able compliance and patient safety.\nAreas Covered in the Session :\nS
 tatutes, Regulations and Definitions\nRegulatory Requirements for INDs
  and IDEs.\nClinical Trials\nClinical Investigators (CI)\nInstitutiona
 l Review Boards (IRBs)\nSponsors and Monitors\nContract Research Organ
 izations (CROs)\nICH-GCP Guidelines\nISO 14155\nList of SOPs and Adequ
 ate Documentation\nKey Elements in the SOPs\nCommon GCP Deficiencies i
 n EU and US\nEnforcement Actions\nLessons Learned\nWho Will Benefit:\n
 Clinical Affairs\nRegulatory Affairs\nQuality Assurance\nResearch & De
 velopment\nConsultants\nContractors/Subcontractors\nSenior Management\
 nAnyone Interested in the Topic\nPrice Tags:\nLive\nSingle Live : For 
 One Participant\n$ 249\nCorporate Live : For Max. 10 Participants\n$ 8
 99\nRecording\nSingle REC : For One Participant - Unlimited Access for
  6 Months\n$ 299\nFor more information and enquiries contact us at\nCo
 mpliance Trainings\n5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Ca
 nada  Customer Support : #416-915-4458  Email : support@compliancet
 rainings.com\nFor more information about this webinar\nhttps://complia
 ncetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1359\nLike Us
  On facebook\nhttps://www.facebook.com/events/800247606712405/?source=
 1&sid_create=616533931\n\nFor more information visit https://medtechiq
 .ning.com/events/webinar-on-good-documentation-practices-for-clinical-
 trials-1
DTSTART;TZID=America/New_York:20150220T130000
DTEND;TZID=America/New_York:20150220T140000
CATEGORIES:webinar
LOCATION:Online
WEBSITE:https://compliancetrainings.com/SiteEngine/ProductDetailView.a
 spx?id=FDB1359
URL:https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?
 id=FDB1359
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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