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In-Depth Testing of Computer Systems Regulated by FDA - Webinar


2017, November 28

Other » Webinar


OVERVIEW
This FDA compliance webinar will leave you with the information needed to create and maintain good documentation that meets FDA compliance standards. FDA requires that all documentation related to GxP (GMP, GLC, and GCP) products be created and maintained in accordance with specific rules.

WHY SHOULD YOU ATTEND

You should attend this webinar if you are responsible for any FDA-regulated data and/or records. All documents need to be created and maintained in accordance with FDA guidelines for good documentation to avoid any issues during an inspection or audit.

AREAS COVERED

FDA Good Documentation Practices
Computer System Validation (CSV)

LEARNING OBJECTIVES

To understand industry best practices.
To understand and avoid potential pitfalls.

WHO WILL BENEFIT

Information Technology Analysts
QC/QA Managers
QC/QA Analysts

SPEAKER

Carolyn Troiano has more than 30 years of experience in computer system validation in the pharmaceutical, medical device, animal health and other FDA-regulated industries. She is currently managing a large, complex data migration, analytics and reporting program at a major financial institution.During her career, Carolyn worked directly, or as a consultant, for many top-tier pharmaceutical companies in the US and Europe. She was responsible for computer system validation across all GxP functions at a major pharmaceutical company.

For more details click on this link:
www.trainingdoyens.com


Venue

Internet - webinar

Organizer

Phone: +1-720-996-1616
Visit organizer website



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