Alan Moon has been a GMP inspector with the UK MHRA since 2013 and conducts inspections globally in areas including sterile manufacturing, non-sterile manufacturing and investigational medicinal products. He is the UK MHRA representative for the Annex 1 revision working group.
Prior to joining MHRA, he worked in the pharmaceutical industry for approximately 20 years in various roles including Quality Control, Quality Assurance and Production, primarily in the manufacture of sterile pharmaceuticals but also various other dosage forms and investigational medicinal products.