About me
Dr Thomson is a consultant providing expert advice on clinical trial design, analysis and interpretation. He spent over 18 years as a regulator in the EU system, where he held a variety of quantitative roles, initially at the UK regulator, MHRA and subsequently at EMA. In his time at EMA he was amongst other roles the main scientific secretariat of the Methodology Working Party, and the Regulatory Chair of ICH E11A and ICH E6 Annex 2.
