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Computer Systems 2021 - Best Practices for Auditing a Vendor of Computer Systems Regulated by FDA
Topics/Call fo Papers
Computerized systems that are used in FDA-regulated environments (i.e., the system “touches” an FDA-regulated product, or a raw material or packaging component used in conjunction with the product during the manufacturing,
Effective and compliant computer system development, testing and validation are critical to any pharmaceutical or FDA-regulated organization.
Developing a strategic approach to vendor audit
Understanding best industry audit practices to ensure FDA compliance
Speaker:
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.
Effective and compliant computer system development, testing and validation are critical to any pharmaceutical or FDA-regulated organization.
Developing a strategic approach to vendor audit
Understanding best industry audit practices to ensure FDA compliance
Speaker:
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.
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Last modified: 2021-01-21 00:57:50