How can we better support sites and patients on our clinical trials?

How can we better support sites and patients on our clinical trials?

By aidan.gannon@longboat.com

Date and time

Wed, 24 Aug 2016 12:00 - 13:00 EDT

Location

MassBio

300 Technology Square Cambridge, MA 02139

Description

Clinical trials are becoming increasingly complex, with twice as many procedures per protocol now than there were in 2003. And Tufts tell us that nearly half of all deficiencies at investigative sites are due to non-compliance.

So how can we better support the busy site staff responsible for collecting the data we need? And is there an better way for study teams to inform, engage and communicate with their sites from initiation through Database Lock and share lessons learned?

And how can we ensure the study participants - our patients - are engaged and empowered throughout the study, so they can feel valued and part of a greater community?

Join the Longboat team for an interactive discussion on how technology can help improve our clinical trials.

The venue will be accessible from 11:30am, with the event to begin at 12 noon. Lunch will be provided.

Organised by

Longboat are a team of highly experienced clinical research professionals, physicians, and technology experts dedicated to generating better study outcomes by providing the people who create the data - study teams, site staff and patients - with the information they need, when they need it - Guided Compliance™.

As the pioneers in the development of assisted protocols, our unique skill set allows us to create innovative and transformational technologies that are integral in bringing novel medicines to patients and their families sooner.

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