The Impact Of CTIS On Research Workflows

About this session

Breakout session. This session will assess the impact of the Clinical Trials Information System (CTIS) on clinical research workflows. Analyze the functionalities, benefits, and potential challenges of CTIS implementation on regulatory processes, transparency, and efficiency. Ensure your site is fully equipped for the transformative implications of CTIS within the clinical research landscape.

Speakers

• CB

  Christopher Bamford

  Director, Clinical Trials Regulatory · IQVIA

  Panelist

• 

  Edyta Maciolek

  Regulatory Affairs Manager · CTR Consulting

  Panelist

• NM

  Natalia Ayas Montero

  Director, Regional Director Submission Lead, Head · MSD

  Panelist

• VL

  Victoria Aniyar López-Abadia

  Medical Director · VCTC

  Panelist

• VL

  Victoria Aniyar Lopez-Abadia

  Medical Director · VCTC

  Panelist