Speaker

Carolyn Troiano

Biography

Carolyn Troiano has more than 35 years of experience in computer system validation and compliance in the pharmaceutical, medical device, tobacco and other FDA-regulated industries. She is currently an independent consultant, advising companies on computer system validation and large-scale IT system implementation projects.

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Carolyn Troiano

21 CFR Part 11, FDA's Guidance for Electronic Records and Signatures Using a Computer System Regulated by FDA

21 CFR Part 11, FDA Guidance for Electronic Records and Signatures Using a Computer System Regulated by FDA

The Future of Clinical Research: Leveraging ICH E6(R3) Updates and Technology Innovation for Success

Emerging FDA Trends in Computer System Validation (CSV)

Risk-Based Approach to Validating IT Infrastructure Used for FDA-Regulated Systems

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Carolyn Troiano

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21 CFR Part 11, FDA's Guidance for Electronic Records and Signatures Using a Computer System Regulated by FDA

21 CFR Part 11, FDA Guidance for Electronic Records and Signatures Using a Computer System Regulated by FDA

The Future of Clinical Research: Leveraging ICH E6(R3) Updates and Technology Innovation for Success

Emerging FDA Trends in Computer System Validation (CSV)

Risk-Based Approach to Validating IT Infrastructure Used for FDA-Regulated Systems

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