(CSV) for FDA-Regulated Computers

Overview:
You'll learn about the various computer system validation deliverables and
how to document them through the entire process, also learn about what
must be done to ensure the system remains in a validated state.

Why should you Attend:
This webinar will describe the policies, procedures, training and other
underlying support elements that are needed to ensure ongoing
maintenance of a system in a validated state.

Areas Covered in the Session:
Security, Access, Change Control and Audit Trail
Policies and Procedures
Training and Organizational Change Management
Industry Best Practices and Common Pitfalls

Who Will Benefit:
Analytical Chemists
Laboratory Managers
Automation Analysts
GMP Training Specialists

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: $150.00

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: compliance4all14@gmail.com