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Compliance for Computer Systems Regulated by FDA - 2020
Date
Oct 12, 2021 - 10:00 AM
Link to Website
Organizer
Netzealous LLC DBA - Compliance4All
Venue
Online Event
Location
Netzealous LLC DBA - Compliance4All,
Fremont,
CA,
US,
ZIP: 94539
Phone: 18004479407
Ticket Price: $ 150.00
Overview:
The Webinar will focus on the importance of ensuring that electronic
record/electronic signature (ER/ES) capability built into FDA-regulated
computer systems meets compliance with 21 CFR Part 11. This includes
development of a company philosophy and approach, and incorporating it into
the overall computer system validation program and plans for individual
systems that have this capability.
Why should you Attend:
This Webinar will help you understand in detail the application of FDA's 21
CFR Part 11 guidance on electronic records/electronic signatures (ER/ES) for
computer systems subject to FDA regulations.
Areas Covered in the Session:
Validation Strategy
System Risk Assessment
GAMP 5 "V" Model
21 CFR Part 11
Electronic Records/Electronic Signatures (ER/ES)
Security, Access, Change Control and Audit Trail
Who Will Benefit:
Clinical Data Managers and Scientists
Analytical Chemists
Laboratory Managers
Automation Analysts
Manufacturing and Supply Chain Managers and Analysts
Computer System Validation Specialists
Speaker Profile:
Carolyn (McKillop) Troiano Carolyn 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.
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: [email protected]
The Webinar will focus on the importance of ensuring that electronic
record/electronic signature (ER/ES) capability built into FDA-regulated
computer systems meets compliance with 21 CFR Part 11. This includes
development of a company philosophy and approach, and incorporating it into
the overall computer system validation program and plans for individual
systems that have this capability.
Why should you Attend:
This Webinar will help you understand in detail the application of FDA's 21
CFR Part 11 guidance on electronic records/electronic signatures (ER/ES) for
computer systems subject to FDA regulations.
Areas Covered in the Session:
Validation Strategy
System Risk Assessment
GAMP 5 "V" Model
21 CFR Part 11
Electronic Records/Electronic Signatures (ER/ES)
Security, Access, Change Control and Audit Trail
Who Will Benefit:
Clinical Data Managers and Scientists
Analytical Chemists
Laboratory Managers
Automation Analysts
Manufacturing and Supply Chain Managers and Analysts
Computer System Validation Specialists
Speaker Profile:
Carolyn (McKillop) Troiano Carolyn 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.
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: [email protected]
Event Categories
Keywords: computer, FDA, medical