How to Comply with 21 CFR 11 Requirements
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Website http://www.compliance4all.com/control/w_product/~product_id=501746LIVE?channel=ourglocal_May_2018_SE |
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Category Electronic Medical Records, electronic health records, medical records online, compliance training webinar, compliance trainings 4 all, fda calibration requirements, Clinical Research Associates
Deadline: May 01, 2018 | Date: May 02, 2018
Venue/Country: Online, U.S.A
Updated: 2018-03-20 14:55:29 (GMT+9)
Call For Papers - CFP
Overview:In this webinar would apply to computerized systems that create source documents (electronic records) that satisfy the requirements in 21 CFR 312.62(b) and 812.Areas Covered in the Session:What are source documents and why are they important? (FDA and ICH GCP E6 Guideline)What are required characteristics for source documents?What is 21 CFR Part 11?How can you apply 21 CFR 11 and ICH E6 to source documents?How EMR Data is used in Clinical investigationsHow to plan electronic source document deficienciesWho Will Benefit:InvestigatorsClinical Research CoordinatorsDevice and Drug Study Clinical Research AssociatesClinical Research Associate ManagersProject ManagersQuality Assurance PersonnelRegulatory Affairs PersonnelSpeaker Profile:Angela Bazigos Seasoned Executive with 40 years of experience in the Life Sciences & Healthcare Industries. Positions include Chief Compliance Officer http://morflearning.com/angelabazigos/. Experience combines Quality Assurance, Regulatory Compliance, Business Administration, Information Technology, Project Management, Clinical Lab Science, Turnarounds and Business Development.Event Fee: One Dial-in One Attendee Price: US$150.00Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: supportcompliance4All.com
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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