Good Manufacturing Practice

• All professionals involved in manufacturing of pharmaceutical drug products
  
• Quality Assurance and Quality Control professionals
  
• Operations and Manufacturing personnel
  
• Validation personnel
  
• Engineers
  
• All levels of management
  
• Service organisations, suppliers, and vendors who serve pharmaceutical industry clients

A general GMP inspections are carried out by regulatory bodies such as MHRA, FDA or EMA, to assess the degree of conformity to prescribed standards of good manufacturing practice and to assess compliance with the relevant regulatory requirements, for example, licence provisions. Most professionals working in organisations that must be GMP compliant are expected to be able to provide an individual or group certificate as a proof of compliance.