Implementing a Robust Data Integrity Program- 2019
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Website https://www.compliance4all.com/control/w_product/~product_id=502329LIVE?channel=ourglocal_Mar_2019_S |
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Category Data review, File format, Storage media, Encryption
Deadline: March 10, 2019 | Date: March 11, 2019
Venue/Country: Online, U.S.A
Updated: 2019-01-21 15:04:31 (GMT+9)
Call For Papers - CFP
Overview:Attendees will be presented with an overview of the audit trails within an application and the content of each one, Also Attendees will be presented with a list of records to identify if they are GMP records.Why should you Attend:The regulatory concern has been responded to by both domestic and foreign governing agencies with the FDA, EMA, MHRA, WHO, and PIC/S all having recently published data integrity standards and guidelines.Areas Covered in the Session:File formatStorage mediaEncryptionUser management (access control)Review of the data life cycleHandling of raw dataUnauthorized accessWho Will Benefit:ProductionEngineering & ValidationFacilities / MaintenanceQuality AssuranceRegulatory AffairsSpeaker Profile:Kelly Thomas has over two decades of cGMP hands-on industry experience in both pharmaceutical and medical device manufacturing operations. Her experience covers all Quality Systems; as well as, all areas of validation; including, process/product validation, facilities validation, CSV and 21 CFR Part 11, test method validation, equipment/automated processes and cleaning validation.Event Fee: One Dial-in One Attendee Price: US$150.00Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: compliance4all14gmail.com
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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