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.
FDA Good Documentation Practices
Computer System Validation (CSV)
To understand industry best practices.
To understand and avoid potential pitfalls.
WHO WILL BENEFIT
Information Technology Analysts
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.
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