Trends for Computer System Validation, Medical Device Compliance and FDA Enforcement
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Website https://www.compliance4all.com/control/w_product/~product_id=502309LIVE?channel=ourglocal_Mar_2019_S |
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Category Clinical Data Scientists, Analytical Chemists, Compliance Managers
Deadline: March 14, 2019 | Date: March 15, 2019
Venue/Country: Online, U.S.A
Updated: 2019-01-21 15:08:27 (GMT+9)
Call For Papers - CFP
Overview:This webinar will focus on the key areas that are most important for protecting the validity of data that is regulated by FDA, and is typically housed electronically in computer systems.Why should you Attend:This guidance was first issued in 1983, and the main points of focus remain consistent today, despite the number of years that have passed and the technology changes that have taken place.Areas Covered in the Session:FDA Regulatory TrendsFDA Response to ChangeRecent FDA findings for companies in regulated industriesRecent trends in technology that need to be addressed in the CSV approachIndustry Best PracticesWho Will Benefit:Clinical Data ScientistsAnalytical ChemistsCompliance ManagersLaboratory ManagersAutomation AnalystsManufacturing ManagersSpeaker Profile:Carolyn (McKillop) Troiano has more than 35 years of experience in the tobacco, pharmaceutical, medical device and other FDA-regulated industries. She has worked directly, or on a consulting basis, for many of the larger pharmaceutical and tobacco companies in the US and Europe, developing and executing compliance strategies and programs.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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