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

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

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.