FDA's New Enforcement of 21 CFR Part 11

Date : 11th July 2019 to 11th July 2019

Place : United States, Fremont

Website :https://www.compliance4all.com/control/w_product/~product_id=502594LIVE?channel=allconferencealerts_Jul_2019_SEO

Contact Person:Event Manager

Description:

Overview: The webinar will have the answers. And using industry proven case studies on how to avoid 483 inspectional observations and warning letters attendees will learn how to prepare their organization for trouble-free Part 11 related inspections. Why should you Attend: There are many questions about the P11 inspection program, e.g., what inspectors are looking at and what major findings are. The seminar will have the answers. In addition, using industry proven case studies on how to avoid 483 inspectional observations and warning letters attendees will learn how to prepare their organization for trouble-free Part 11 related inspections. Areas Covered in the Session: FDA's past inspection and enforcement practices Reason for changing inspections and enforcement FDA's new interpretation: learning from FDA inspection reports How can the new requirements be implemented in your company Who Will Benefit: IT Managers and System Administrators QA Managers and Personnel Validation Groups Software Developers Validation Professionals Speaker Profile Ludwig Huber Ph.D., is the director and editor of Labcompliance the global online resource for validation and compliance. He is the author of the books "Validation and Qualification in Analytical Laboratories" and "Validation of Computerized Analytical and Networked Systems, Informa Healthcare". Event Fee: One Dial-in One Attendee Price: US $190.00 Contact Detail: Compliance4All DBA NetZealous, Phone: +1-800-447-9407 Email: [email protected]

FDA's New Enforcement of 21 CFR Part 11 will be held in Fremont,United States on date 2019-07-11

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Deadline for abstracts/proposals : 9th July 2019

Keynote Speakers :

Venue :Fremont, CA, USA

Check the event website for more details.