iRegulatory Ltd provides the services of Dr. Martin Moxham as a consultant in EU pharmaceutical regulatory affairs. Martin has >24 years’ experience in this field, including >17 years in managerial positions and >10 years in consulting roles.
Martin is skilled in the interpretation of EU regulatory guidelines and precedents, and their application to pharmaceutical product development. In addition, he has good scientific writing skills; he has the ability to summarise and discuss complex concepts and data, and to prepare written arguments and justifications that are clear and cogent.
Martin can add value to client projects by helping to identify areas of potential concern to the regulators, and assisting clients to address issues proactively during development and in subsequent regulatory submissions.