Partnering with Patients to Streamline Trial Operations: Protocol to Regulatory Submission in 60 days

概要

This Solution Provider Webinar is brought to you by DIA in cooperation with

In This Webinar

Learn how patients and patient advocacy organizations can be directly enabled as powerful partners to facilitate all stages of DCT deployment, from protocol design, recruitment, engagement to dissemination of results. This webinar will share best practices and real-world examples addressing multiple therapeutic areas and patient populations.

学習目的

At the conclusion of this webinar, participants should be able to understand:

Recognize the value of obtaining patient input at all stages of the product development lifecycle can streamline data collection, research operations, and actionability of the results
Create effective networks with service providers and patient advocacy organizations to incorporate patient-generated data and patient centric insights across the product development lifecycle
Identify opportunities to implement a digital lifecycle approach to overcome challenging scenarios such as aggressive timelines, ultra-rare and geographically distributed patient populations, or the need to measure qualitative endpoints

Partnering with Patients to Streamline Trial Operations: Protocol to Regulatory Submission in 60 days

概要

In This Webinar

特集トピック

学習目的

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