161 Mission Falls Lane, Suite 216,

Fremont,

CA,

US,

ZIP: 94539

Phone: 18004479407

Overview:
In this webinar speaker will discuss the best practices necessary to develop
an integrated laboratory and business data collection, analysis and
reporting computer system validation program.

Why should you Attend:
Those users accessing the business system must also not be able to enter
or alter data directly into the laboratory system, unless it is clearly a
requirement based on the process being followed. 

Areas Covered in the Session:
Identify the key input and output points that will warrant greater scrutiny
as the integrated system is tested and validated
Discuss the steps for validating systems, along with the key documentation
associated with maintaining the systems in a validated state, while
minimizing costs
Learn how to leverage these practices across all systems by creating a
standardized program for integrating FDA-regulated and non-regulated
systems
Understand the additional training that must be provided to business and IT
staff involved in the integration process

Who Will Benefit:
Clinical Data Managers and Scientists
Analytical Chemists
Laboratory Managers
Automation Analysts

Speaker Profile:
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.

Event Fee: One Dial-in One Attendee Price: US$150.00

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: [email protected]