GMP for Pharmaceutical Excipients | Rephine Symposium 2021

Topic: Biopharmaceuticals, Manufacturing

The webinar gives an overview about the current GMP regulations for pharmaceutical excipient and the most effective approach for qualification of pharmaceutical excipient suppliers.

Based on risk assessment the qualification process can include a number of options ranging from documental review, desktop assessment, remote and onsite audits. The qualification approach and associated criticalities or potential non conformities will be discussed from an auditor’s perspective.

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