Profile of Andrew P. Marr

Andrew Marr, Marr Consultancy

Andrew Marr

30 years in the Pharmaceutical industry in Regulatory Affairs and Regulatory Operations. 10 years in Regulatory Affairs including UK, US, Preclinical and CMC regulatory roles. 15 years in Regulatory Operations with business-side responsibilities for the development, implementation and process optimisation of regulatory document management and publishing systems and electronic submission to regulatory agencies. 10 years at the forefront of standards and process development for electronic interchange between industry and regulator, on a worldwide basis.

  • Strategy consultant, highly respected in the pharmaceutical sector.
  • Leading consultant on the requirements and business processes for the Extended Eudravigilance Medicinal Product Dictionary (XEVMPD) and Identification of Medicinal Products (IDMP)
  • Extensive expertise in electronic submission requirements and processes in Europe and US gained from pivotal involvements throughout their development and successful implementation.
  • Extensive experience of the Product Information Management (PIM) programme gained as industry lead since its inception.
  • Extensive network and reputation with regulators, industry, service providers and software vendors working in these spaces

Andrew Marr on LinkedIn

Marr Consultancy is a limited liability company registered in England and Wales. Registered No.07439196