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Welcome to the Wednesday edition of the Clinical Leader newsletter, focusing on Decentralized Trials and Trial Management. Update your topic preferences to receive additional Clinical Leader newsletters on:
- Clinical Sites | Patient Centricity | Patient Recruitment (Monday)
- Clinical Trial Technology (Tuesday)
- Outsourcing Models | Regulatory & Compliance (Thursday)
- Clinical Data Management & Analytics | Trial Monitoring (Friday)
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How Can You Help Sites Manage Training And Education On DCT Technologies?
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Video |
Clinical Leader Live
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Chief editor Ed Miseta recently spoke to three site experts about the pain points of DCTs, including costs, budgeting, training, support, staffing, resources, and more. In this video, Jimmy Bechtel of SCRS, Karri Venn of Centricity Research, and Brad Hightower of Hightower Clinical discuss the training challenges that arise at sites from the implementation of new DCT technologies.
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Understanding Options In Direct-To-Patient Clinical Supply
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Video |
Catalent
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Direct-to-patient clinical supply enables clinical trial participants to receive their treatments in the convenience and comfort of their own home and reduces, or even eliminates, the need to travel to a clinical site.
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Optimizing The Decentralization Of Clinical Trials
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Article |
By Jennifer Duff, Clinical Development Solutions, Merative
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Decentralizing aspects of the clinical trial is a natural evolution, with the caveat being that the COVID-19 pandemic helped accelerate that evolutionary process by several years. But learn why decentralization is not necessary for all types of research.
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How To Implement Successful Remote Studies
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e-book |
OpenClinica
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The emphasis on decentralized clinical trials (DCTs) has been growing for some time, but how can we execute these types of trials for more successful outcomes that provide better data, faster? Read this e-book to learn more.
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Unpacking IRB Innovations For Decentralized Clinical Trials
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Article |
By James Riddle, Advarra
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This blog highlights how IRBs can simplify review of electronic patient reported outcome (ePRO) and electronic clinical outcome assessment (eCOA) materials to streamline study start-up without impacting the review quality.
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Decentralized Trials For Duchenne Muscular Dystrophy
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Case Study |
MRN - Medical Research Network
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Working closely with a global biotechnology company on a mission to engineer precision genetic medicine for rare diseases, MRN has delivered more than 180 home visits per month to keep trials running across a vulnerable pediatric population during the COVID-19 pandemic.
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Beyond Nuclear Genetics: Let’s Think Differently About CNS Disease Targets
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Guest Column |
By Amy Ripka, Ph.D., Lucy Therapeutics
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Nuclear genes with mutations remain the primary focus for selecting biological drug targets, but we have yet to see a drug come to market from a genetically validated target that can arrest or reverse diseases such as Parkinson’s. We need to expand our research to explore the essential drivers, genetic or otherwise, that switch our cells from order to disorder or from function to dysfunction.
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A Smart Solution To Clinical Supply Management
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Application Note |
By Carolyn Timpany, Lisa Spence, and Ed Groleau, PCI Pharma Services
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Discover a supply management solution that ensures efficient delivery of clinical trial materials worldwide, while navigating the challenges of more complex study designs and the ever-evolving regulatory landscape.
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Selecting A Study-Specific Protocol Training Strategy
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Article |
By David Hadden, Pro-ficiency
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When it comes to clinical protocol training, read why research sites and sponsors need to determine what their ultimate goals are to correctly identify the best training tools for the job.
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Are We Ready For A Unified Clinical Platform?
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Webinar |
Cognizant
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Industry experts from Eli Lilly and Cognizant share their perspectives on the process and building blocks of end-to-end clinical development, the essential elements of a unified clinical platform, and the benefits and challenges involved in realizing the vision of a unified clinical platform.
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Flexibility And Speed In Early-Phase Clinical Trials
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Article |
By Crista Casey, Cmed Clinical Research Services
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Explore how simple language adjustments to clinical trial protocol, intelligent use of decentralized services, and real-time data visibility via intuitive technology can reduce project timelines by weeks or even months.
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Nephrology Patient Safety Starts In The Clinical Trial Setting
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Article |
Biorasi
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Is the clinical trial setting the best environment to ensure a patient’s safety? Dr. Jamie P. Dwyer discusses how nephrology clinical trials identify future patient risk factors for medication and treatment in the real-world setting.
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Contract Pharmaceutical Blister Packaging Services
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Product |
Ropack Pharma Solutions
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According to recent market surveys the global blister packaging market reached a value of $22.7 billion (U.S.) in 2021. Looking forward, the market is set to reach $32.2 billion (U.S.) by 2027, exhibiting a CAGR of 5.8% during 2022-2027.
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Cell And Gene Therapy Services
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Brochure |
LabConnect
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Learn how LabConnect is transforming central lab services and mastering every aspect of sample tracking, complex testing, logistics, and data management.
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