• Awareness that GMP is applicable to all roles involved in the manufacturing of (investigational) drug products, including external manufacturer / CMO and other vendors
• Setting up and managing compliance with quality standards for both the internal organisation as the vendors
• Complying to GMP and quality standards makes processes efficient, accurate, and reliable.
• Ensure the safety of the subjects and patients by making sure the (investigational) drugs are consistently produced and controlled according to (GMP) quality standards by vendors
• Understand how to perform quality oversight on their production and control.
• Understand oversight elements such as vendor selection, quality visits, and clear communication processes

This training is applicable for the Quality department, the QMS team, management of pharmaceutical and biotech companies, drug product development leaders, clinical study supply leaders, CMC leaders, and all others involved in quality oversight.