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During an ISO audit, the auditor will be asking for records or evidence the quality System being audited has effectively maintained the records required. For example, when an auditor is reviewing the corrective and preventive action system, he or she will be looking for a CAPA Report to provide evidence that the CAPA system has met the requirements for section 8.52 Corrective Action and 8.5.3 Preventive Action.

In this webinar the speaker will discuss about the regulatory compliance for complaint handling in various industries like pharmaceutical, medical device.

Get educated on lean configuration, quality system Regulation, 21 CFR Part 820, and ISO 13485 as it applies to Corrective and Preventive Action.

Tips to learn how to manufacture products with Zero defects, types of flaws in manufacturing requirements, and defect mitigation methods.