A Regulatory Perspective: Integrating PIM into the Product Lifecycle

Pharma IQ speaks to Andrew Marr, Director of e-Regulatory Development and Global Regulatory Operations and Co-Chair of the PIM Steering Committee on behalf of the EFPIA. This interview addresses the latest developments in Project Information Management (PIM) and gives an overview of why it is important to prepare before implementing PIM. Dr Marr outlines the main challenges faced and the lessons learned so far by trial groups – and talks in depth about the advantages to be gained from implementation. Dr Marr will be speaking at the upcoming Successful eCTD Lifecycle Management conference, which will take place from 13th – 15th September in Prague. For details of how to get involved, please visit www.ectdevent.com, email enquire@iqpc.co.uk or call +44 (0)207 368 9300.