Quantifying the Collection of Non-Core and Extraneous Core Protocol Data and its Relationship with Clinical Trial Performance

About this session

Session: TUESDAY MORNING PLENARY SESSION: REINVENTING CLINICAL DEVELOPMENT & CONVERGING RESEARCH WITH CLINICAL CARE

This panel discussion provides perspectives and updates on a collaborative research study looking at optimizing non-core and extraneous clinical research data collection practices, with the aim to reduce patient and site burden. The panel will explore considerations that helped define the study methodology and insights expected from the study findings that will inform new protocol design strategies.

Speakers

• EB

  Emily Botto

  Sr Research Analyst · Tufts Center for the Study of Drug Development

  Moderator

• PD

  Paul P Duffy

  Head, Global Clinical Site Partnerships · MSD Ltd

  Panelist

• JL

  Joachim Lovin

  DCT Specialist · Novo Nordisk A/S

  Panelist