This 5 day fully residential course, provides the most comprehensive training & certification for Auditors and Lead Auditor auditing GMP Pharmaceutical sites.
The course covers the role of an auditor to plan, conduct, report and follow up an audit of a pharmaceutical quality management system audit in accordance with ISO 19011. It gives you the skills to plan, conduct, report and follow up an audit of a pharmaceutical quality management system to establish conformance (or otherwise) against ICH Q10 and in accordance with ISO 19011. Learners will be assessed through practical tasks, activities and must also pass the IRCA PR325 written examination that lasts 2 hours.
The course covers the role of an auditor to plan, conduct, report and follow up an audit of a pharmaceutical quality management system audit in accordance with ISO 19011. It gives you the skills to plan, conduct, report and follow up an audit of a pharmaceutical quality management system to establish conformance (or otherwise) against ICH Q10 and in accordance with ISO 19011. Learners will be assessed through practical tasks, activities and must also pass the IRCA PR325 written examination that lasts 2 hours.
