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Global decentralized studies will become a standard clinical trial design approach

The Pharma Data

After a year of unprecedented disruption in the clinical research industry, 2021 is set to be another transformative year for sponsors and contract research organizations (CROs), according to John Reites, president of Thread, a technology and service provider focusing on decentralized clinical research. Source link: [link].

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How Can You Manage the Complexity of Early Phase Clinical Development?

XTalks

In the ever-evolving landscape of pharmaceutical development, the complexity of early phase clinical trials is increasing. The company partners with small and large biopharma and medical device and diagnostic companies to optimize early clinical development through excellence in study design and execution.

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Reuters Events: Pharma & Patient USA | October 15-16, 2024

Pharma Marketing Network

You must integrate and co-create from the outset, from clinical design to commercial execution to boost adherence, trial participation and create exceptional outcomes. YOU are the patient advocate in your company, so overturn tokenistic gestures into meaningful actions that prioritise patients over patents. This starts now.

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Common Pitfalls in Preparing an IND Application

Advarra

Using nonclinical data or manufacturing information that doesn’t adequately support the clinical protocol hurts the IND application. It’s critical to ensure all nonclinical data supports the clinical design and provides adequate justification of the desired labeling claims – including basic exposure data. Inadequate Support.