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DTSTART:19700308T020000
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UID:2140535:Event:470954
DTSTAMP:20260517T075604Z
SUMMARY:Clinical Data Management (CDM)
DESCRIPTION:Clinical data management (CDM) is paramount for a successf
 ul research. After all, Garbage In, Garbage Out (GIGO).\nCDM involves 
 all aspects of collecting, processing, and interpreting information. T
 here are many types of computer applications and database systems to s
 upport data collection and management. However, there are elements of 
 CDM that apply across the board.\nReview and approval of drugs or devi
 ces by regulatory agencies requires the assumption that the data prese
 nted are valid and reliable. Integrity of the data is paramount to ens
 ure confidence in the results and conclusions you will make.\nThis sem
 inar is based on FDA E6 GCP Guidelines which are the basis of effectiv
 e data quality management. Even if your research is not FDA regulated,
  the information you learn in this course will help to ensure a robust
  data collection and management plan.\nThe information conveyed in thi
 s course will also assist investigators in setting up processes for sm
 oother data monitoring and auditing.\nExamples of CRF’s and required
  documentation will be presented. Data collection and preparation tech
 niques will also be demonstrated. Additionally, this workshop will pro
 vide you with the knowledge and tools needed to assure a CDM plan that
  holds up when the inevitable deviations from protocol occur.\nDisclai
 mer: This seminar is not endorsed by, directly affiliated with, maint
 ained, authorized, or sponsored by the Society for Clinical Data Manag
 ement or any other clinical research society. All products, processes,
  and company names are the registered trademarks of their original own
 ers. The use of any trade name or trademark is for identification and 
 reference purposes only and does not imply any association with the tr
 ademark holder of their brand.\nLearning Objectives:\n\nRegulatory gui
 delines for Clinical Data Management\nBest practices for data collecti
 on\nCDISC/CDASH/STDM standards\nResponsibilities of personnel\nCase re
 port form criteria\nMaintaining confidentiality of data\nData storage 
 and transferability\nData preparation and quality assurance for accura
 cy\nData monitoring plan criteria\n\nWho will Benefit:\n\nStudy Invest
 igators\nData managers\nData processors\nStatisticians\nSite Personnel
 \nClinical Research Associates\nClinical Project Managers/Leaders\nStu
 dy Sponsors\n\n\nFor more information visit https://medtechiq.ning.com
 /events/clinical-data-management-cdm-1
DTSTART;TZID=America/New_York:20220420T100000
DTEND;TZID=America/New_York:20220421T160000
CATEGORIES:webinar
LOCATION:online
WEBSITE:https://www.complianceonline.com/clinical-data-management-cdm-
 seminar-training-80552SEM-prdsm?channel=MedTech%20I.Q
URL:https://www.complianceonline.com/clinical-data-management-cdm-semi
 nar-training-80552SEM-prdsm?channel=MedTech%20I.Q
CONTACT:8887172436
ORGANIZER:Complianceonline
ATTACH;FMTTYPE="image/jpeg":https://storage.ning.com/topology/rest/1.0
 /file/get/10038456680?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN=Complianc
 eOnline:https://medtechiq.ning.com/profile/Referral512
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