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Best Practices to Help you Pass an FDA Computer System (Validation)
Presented By Netzealous LLC DBA - Compliance4All
Friday, December 7th at 9:00am PST
Online sale ends: 12/07/18 at 8:00am PST
Online
161 Mission Falls Lane, Suite 216,
Fremont, CA 94539
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Talent
Description
Overview: This webinar will help you understand the FDA's current thinking on computer systems that are validated and subject to inspection and audit. Areas Covered in the Session: 21 CFR Part 11, Electronic Records/Electronic Signatures (ER/ES) Data Archival to ensure security, integrity and compliance Validation Strategy that will take into account the system risk assessment and system categorization (GAMP V) processes Recent FDA findings for companies in regulated industries Who Will Benefit: Anyone who is involved in the development, testing, manufacturing, storage, handling and distribution of product must understand and conform to FDA requirements for data quality and integrity, and computer system validation (CSV) Finally, anyone who is acting as a consultant or contractor to a company in an FDA-regulated industry should attend to ensure they are able to bring the most current knowledge and expertise to their assignment Speaker 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$290.00 Contact Detail: Compliance4All DBA NetZealous, Phone: +1-800-447-9407 Email: support@compliance4All.com Additional Information
One Dial-in One Attendee
Price: $290.00
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Presented By
9:00am to 12:00pm
General Admission: $290.00
All Ages
50 18004479407 UPCOMING EVENTS
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