In this workshop you will get a technical introduction into digital signatures, an overview of signature legislation and an explanation of the requirements from 21 CFR Part 11 (Code For Regulations) of the FDA (Food and Drug Administration). You will understand how to fulfill these requirements using PDF documents and how to reach Part 11 compliance with an appropriate IT solution.

This workshop is tailored for Quality-Managers and Compliance-Experts as well as IT Managers in Life-Sciences companies.

Duration 1 day

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