Regulatory Information Management (RIM): Delivering Better Efficiencies Across Operations

Sponsored by: AMPLEXOR Life Sciences

Focused on:

    Date: 26 February


    Time: 3PM London/10AM New York

    Automating Multiple Systems and Streamlining Compliance Reporting

    In the past, automation used to be focused on standardizing your way of working in such ways that manual processes could be replaced by machines, resulting in significant efficiency gains. Though this is still an important aspect, automation has matured up to a stage where informed decision-making based on high quality data lies within reach.

    With the introduction of product information data standards such as IDMP, a new generation of Regulatory Information Management (RIM) systems and better integration of information flows within business processes this interoperability enables organisations to provide the right information to the right people at the right time, to make the right decisions.

    In this webinar, Frits will provide you with valuable insights on where he envisions the industry going and how to get started yourself, all based on best practices and real-life experiences.

    Presented by

    Frits Stulp,

    Managing Director, Iperion Life Sciences Consultancy

    Frits is Managing Director of Iperion Life Sciences Consultancy and IDMP SME. He has more than 18 years of experience in the Life Sciences industry. As a project manager, he specialized in the management of IT projects for regulatory compliance and has been the program manager of the first completed IDMP implementation program. Frits serves several clients as IDMP program advisor. He has been a member of the EMA ISO IDMP Task Force and is an active promoter of IDMP at conferences and webinars.

    Key Learning Objectives


      • Quality
      • Regulatory Affairs
      • Document Management
      • Quality Assurance