Webinar on-demand: Ensuring Regulatory Compliance and Quality in Direct-to-Patient Clinical Trials

By Mike Sweeney; Paul Bodfish |

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

About the Authors

Portrait of Mike Sweeney

Mike Sweeney

Senior Director, Patient Centric Logistics
World Courier
Mike is responsible for the development and product management of World Courier’s specialty service offerings across 140 company-owned offices in 50+ countries, with focus on patient-centric areas such as Direct-to-Patient services. Since joining World Courier in 1992, Mike assumed a number of positions within US operations, customer service, training, compliance, marketing, sales and clinical trials management. He progressed to senior roles, including director of US customer service/operations, director of new service development and director of regional accounts, prior to transitioning into a global IT leadership position and most recently into his current role in 2015.
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