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Through a series of interactive sessions and hands-on workshops, become familiar with the World Health Organisation (WHO) Good Distribution Practices (GDP) for Pharmaceutical and Medical Device Products, in order to help you ensure compliance.

Through a series of discussion-based sessions and interactive workshops, learn how to help your organisation demonstrate Good Manufacturing Practice (GMP) compliance using ISO 22716.  Build a strong foundation of knowledge and skills.Course Topics:Overview of GMP and the StandardClause 3: Personnel RequirementsClause 4 and 5: Premises and Equipment RequirementsClause 6 and 12: Raw and Packaging Materials including subcontracting RequirementsClause 7 and 8: Production and Finished products requirementsClause 9: Quality Control Laboratory requirementsClause 10, 11 and 13: Treatment of product that is out of specification including Deviations and Waste management requirementsClause 14: Complaints and recalls requirementsClause 15 and 17: Change Control and Documentation requirementsClause 16: Internal audit requirementsLearning Review and Summary

Through interactive workshops and audit role play, learn to audit your Cosmetic GMP's, according to ISO 22716:2007 and ISO 19011:2018 guidance. Course Topics:Clause 3: Personnel RequirementsClause 4 and 5: Premises and Equipment RequirementsClause 6 and 12: Raw and Packaging Materials including subcontracting RequirementsClause 7 and 8: Production and Finished products requirementsClause 9: Quality Control Laboratory requirementsClause 10, 11 and 13: Treatment of product that is out of specification including Deviations and Waste management requirementsClause 14: Complaints and recalls requirementsClause 15 and 17: Change Control and Documentation requirementsClause 16: Internal audit requirementsHow to Audit According to ISO 19011Learning Review and Summary