complex 
Worldwide Clinical Trials
APRIL 3, 2024
Complying with Unique Radiopharmaceutical Regulations The regulatory landscape for radiopharmaceuticals is intricate, reflecting the drugs’ complexity. The post Strategies for Successful Navigation of Complex Radiopharmaceutical Trials appeared first on Worldwide Clinical Trials.
Pharmaceutical Technology
APRIL 18, 2024
Discover the groundbreaking patent granted to Foghorn Therapeutics Inc for compounds targeting BAF complex-related disorders. Learn about the specific structure outlined in the claim and its potential in medical treatments.
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Rethinking Clinical Trials
APRIL 27, 2023
The chapter, “ Intervention Delivery and Complexity ,” illustrates that—although an intervention may be simple—the actual delivery of the intervention may be complex due to factors such as new workflows, special training of frontline staff, and the number of components in the intervention.
Rethinking Clinical Trials
APRIL 21, 2023
Intervention Complexity Calculator The Intervention Complexity Calculator was developed as a standard tool to capture intervention complexity with the intent to enhance communication challenges of intervention delivery. For further details, see the Living Textbook Chapter on Intervention Complexity.
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As the development pipeline for new drugs continues to grow, biopharmaceutical companies are re-evaluating how to best manage and balance resources across an increasing number of development projects and complex clinical trials.
Bio Pharma Dive
FEBRUARY 20, 2024
Why clinical pharmacology is critical to accelerating drug development, and how it can help drive value in a complex and rapidly evolving landscape.
pharmaphorum
APRIL 9, 2024
Navigating the complex path towards commercialising In Vitro Diagnostics (IVDs) can be challenging. Learn more about the intricate process involved in bringing early diagnostic tools to market.
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The sourcing of commercial drugs for use in clinical trials either as a comparator, rescue or co-medication can be a complex process. Choosing the right partner with global sourcing, regulatory, quality and clinical packaging expertise can provide the necessary guidance to help sponsors successfully navigate these challenges.
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When a CRO is bidding on a project where clinical supplies will be one of the aspects to manage on behalf of the client via a partner, leveraging the expertise of a chosen clinical supply partner can be a valuable resource in demonstrating the CRO’s understanding of and ability to deliver upon critical drug-supply related aspects of the project, and (..)
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White paper that delves into the complex topic of Decentralized Clinical Trials and how to master them within the confines of FDA Regulations
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The global landscape of clinical trials is rapidly changing as studies become more complex. An increasing number of sponsors are seeking enhanced flexibility in their supply chains to address a variety of clinical supply challenges, including patient demand and reducing delays.
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Clinical trial data management is increasingly challenging as studies grow in complexity. Quickly accessing and analyzing study data is vital for assessing trial progress and patient safety. In this paper, we explore real-time data access and analysis for proactive study management.
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