Compliance for Electronic Records and Signatures 2018
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Website http://www.compliance4all.com/control/w_product/~product_id=501772LIVE?channel=ourglocal_Apr_2018_SE |
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Category Healthcare trainings, medical trainings, food health, healthy courses
Deadline: April 05, 2018 | Date: April 06, 2018
Venue/Country: Online, U.S.A
Updated: 2018-02-20 14:02:56 (GMT+9)
Call For Papers - CFP
Overview:This webinar demystifies Part 11, and get you on the right track for using electronic records and signatures to greatly increase productivity.Areas Covered in the Session:Which data and systems are subject to Part 11What Part 11 means to you, not just what it says in the regulationAvoid 483 and Warning LettersExplore the three primary areas of Part 11 compliance: SOPs, software product features, and validation documentationEnsure data integrity, security, and protect intellectual propertyWho Will Benefit:ITQAQCLaboratory StaffManagersGMP, GCP, GLP ProfessionalsSpeaker Profile:David Nettleton, is an FDA Compliance Specialist for 21 CFR Part 11, HIPAA, and Computer System Validation. His latest book is "Risk Based Software Validation - Ten easy Steps" that relates to the development, purchase, installation, operation and maintenance of computerized systems used in regulated applications. He specializes in performing gap analysis, remediation plans, SOP development, vendor audits, training, and project management.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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