How to Validate Automated Pipelines Under CSA — 3-Hour Course
A 3-hour course on validating CI/CD pipelines and automated workflows under CSA — challenge-based testing, automated evidence, and maintaining audit readiness in rapid-release environments.
Instructor
Carolyn Troiano
FDA Compliance & Computer System Validation Consultant
What You'll Learn
About the event
About this event
Automated pipelines introduce speed, volume, and change rates that overwhelm traditional validation approaches. This 3-Hour course teaches teams to validate CI/CD pipelines, integrations, and automated workflows while preserving data integrity and risk-based validation discipline.
Without the right controls, automated systems drift, evidence becomes unreliable, and compliance collapses quickly during inspections. Challenge-based testing and automated test evidence are essential, yet many teams lack a structured method. This course provides an achievable assurance model that supports rapid development without weakening audit readiness.
This is Module 3 of the Practitioner Course "Digital Validation and Cloud Assurance: Validating SaaS, PaaS and Automated Pipelines under CSA."
Code: SEM13453
Curriculum
Requirements
- QA, Validation, IT, Cloud Engineering, and Automation professionals
- Applicable to R&D, digital development, lab informatics, and compliance teams
Meet Your Instructor
Carolyn Troiano
FDA Compliance & Computer System Validation Consultant
Carolyn Troiano has more than 45 years of experience in computer system validation in the pharmaceutical, medical device, biotechnology, tobacco, and other FDA-regulated industries. She is currently an independent consultant, advising companies on FDA compliance, Computer System Validation (CSV), and large-scale IT system implementation projects. Carolyn participated in the FDA/Industry Partnership to develop 21 CFR Part 11, the FDA's Guidance for Electronic Records and Electronic Signatures. During her career she has provided training on CSV, 21 CFR Part 11, Data Integrity, and many other compliance topics of interest to the life science industries.
Event Details
Format
Recorded Webinar
Duration
3 hours
Certificate
Included
Access
Lifetime
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