• The Role and Responsibilities of the Qualified Person
  
  
• EU law and the Role of the Qualified Person
  
  
• Batch Certification : Annex 16 in Practice
  
  
• Batch Record Review
  
  
• Refresher Training for Qualified Persons
  
  
• Investigational Medicinal Products : The Role of the Qualified Person
  
  
• The Qualified Person and Active Ingredients
  
  
• Qualified Person and Professional Development Training

Module 1      Pharmaceutical Law and Administration

Module 2      Medicinal Chemistry and Therapeutics

Module 3      Pharmaceutical Formulation and Processing

Module 4      Pharmaceutical Microbiology

Module 5      Active Pharmaceutical Ingredients

Module 6      Mathematics and Statistics

Module 7      Analysis and Testing

Module 8      Pharmaceutical Packaging

Module 9     Quality Management Systems

Module 10     Practical Module (formulation, manufacturing, analysis)

Module 11     Investigational Medicinal Products

Module 12     The Role and Professional Duties of a Qualified Person