Ensuring Regulatory Compliance and Quality in Direct-to-Patient Clinical Trials

Published: Jan 31, 2017

In this webinar, World Courier and Medical Research Network guide participants through the key regulatory considerations when planning direct to patient trials, as well as providing practical examples to ensure that the quality of your trial delivery is maintained.

This webinar will help participants to:  

Understand what regulatory components need to be considered, and how this may differ regionally and by country.
Understand how to identify and mitigate risks through collaboration, advance planning and clearly defining roles and responsibilities.
Gain insights into what specific challenges can occur with direct to patient trials and how these might be mitigated.
Learn about practical approaches to the evolving regulatory landscape that governs direct-to-patient service models

Author
Mike Sweeney
Mike Sweeney
Senior Director, Global Service Development
World Courier Management
mtsweeney@worldcourier.com
Author
Paul Bodfish
Paul Bodfish
VP Corporate Services
MRN