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Master Production Record Requirements - Webinar By GlobalCompliancePanel

This program will address the 21CFR and Eudralex Volume 4 requirements and interpretation, as well as FDA Guidance regarding the creation, review and approval, and control of Master Production Records

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Webinar on Specification Development - Webinar By GlobalCompliancePanel

A good specification not only defines the product and process being purchased by the customer, but also serves as an extension of the purchasing contract

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Risk-Based Validation for GxP Facilities - Webinar By GlobalCompliancePanel

This presentation teaches a practical methodology for creating and applying Risk-Based Equipment Validation. It shows an example of how this process may be integrated into a facility Master Validation Plan

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