Eric has worked in the pharmaceutical sector for over 15 years, since completing his pharmacist training in the NHS. He is an eligible EU Qualified Person, responsible for supply chain audit oversight and batch release for clinical and commercial products. Eric has worked with a broad range of sterile and non-sterile dosage forms including orphan products as well as time critical sterile and veterinary products. He holds leadership roles in quality, delivering a green field manufacturing facility design project, GMP licence applications and building brand-new quality teams.    

Peter has over 15 years’ experience in the pharmaceutical industry. Qualifying as a pharmacist in 2004, he worked at the Institute of Cancer Research on pharmacogenomic and drug discovery, before moving into commercial and clinical sterile and non-sterile production roles in the UK NHS and commercial organisations. Since 2009, he has worked in Quality roles covering dosage forms, including radiopharmaceuticals and ATMPs. Gaining QP status in 2014, Peter performed batch release for large and small-scale pharmaceutical EU organisations, before continuing as a consultant, overseeing projects including facility builds, FDA remediation, training and QMS implementation.