Business Continuity Planning for [Computer Systems] Operations

Overview:
Computer system validation has been regulated by FDA for more than 30
years, as it relates to systems used in the manufacture, testing,
distribution and management of a product in the pharmaceutical,
biotechnology, medical device, animal health, tobacco and other regulated
industries.

Why should you Attend:
The attendee will also learn how to develop a standard approach to
planning, executing and documenting efforts that involve recovery of
day-to-day business operations and data in a manner that complies with
FDA guidelines. Some people may be new to the concept of validation and
FDA regulation, and will have to be coached on how to follow any
necessary procedures required for compliance.

Areas Covered in the Session:
Gain an understanding of disaster recovery and business continuity
planning
Develop the ability to apply FDA compliance requirements when
developing a disaster recovery and business continuity plan
Understand the best practices for developing a disaster recovery and
business continuity plan

Who Will Benefit:
Information Technology Analysts
QC/QA Managers and Analysts
Clinical Data Managers and Scientists
Compliance Managers
Lab Analysts and Managers
Computer System Validation 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: US $150.00

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com