DIA News Roundup
Oracle Health Sciences announces Clinical One, its cloud-based eClinical platform being built from the ground-up to address the needs of the entire drug development lifecycle. Oracle also launched its first capability on the new platform, Oracle Health Sciences Clinical One Randomization and Supplies Management Cloud Service, which features an intuitive user interface, enabling clinical teams to design, validate and deploy a study more efficiently.
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Introducing CUBE™ - A Transformative IRT Solution by Bracket
CUBE is a clinical IRT solution that lets biotech and pharma sponsors of all sizes deploy studies in just 1 to 2 weeks! With CUBE, you can access all the benefits of an IRT without the time and cost constraints. Benefit from rapid and advanced deployment and a User Acceptance-based and built IRT.  Stop delaying and start deploying now > |
Clinical trial recruitment, engagement, and technology company BBK Worldwide (BBK), has released results of a data analysis across a broad spectrum of trials. The findings confirm the premise that alleviating site staff of many of the mechanical aspects of clinical trial patient management allows more time for personal patient care, creating an enhanced clinical trial experience for patients and site staff alike.
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Minimal Residual Disease Detection: Key Considerations for Clinical Development in Oncology
Live Webcast: Thursday, June 29 at 11:00am EDT  Register now |
The Veeva 2017 Unified Clinical Operations Survey found that nearly all respondents (99%) report at least one major challenge with their clinical applications, most often stemming from application and process silos where 69% cite integrating multiple applications as their biggest issue. Most say (76%) unifying their applications will drive improvements in three or more important areas, including study speed and quality.
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Capturing Continuous Glucose Monitoring Advantages
Live Webinar: Wednesday, June 28 at 11:00am EDT  Register now |
Bioclinica’s Clean Patient Optics™ is a fully-validated clinical trial software solution that provides insights to patient data to improve data cleaning for accelerated database lock and clinical trial timelines.
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Coming to terms with Patient Centricity
Live Webinar: Tuesday, June 20 at 12:00pm EDT
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DIA executives discuss the regulatory trends on tap for discussion at the meeting this week.
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A New Paradigm: Cutting-edge Processes and Analytics in Site and Patient Selection
Live Webinar: Thursday, July 20 at 11:00am EDT  Register now |
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Shortening Biosimilar Development: A Case Study Integrating Early Clinical (Phase I) with late phase (Phase III) Biosimilars Development
Live Webinar: Thursday, June 27 at 11:00am EDT
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Blog Posts
Dr. Jonathan Rowe, Executive Director and Head of Clinical Development Quality Performance and Risk Management, at Pfizer discusses how they are leveraging predictive models to manage study risk and quality.
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Selecting and Auditing a Technology Vendor for Biopharmaceutical Development
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Other News
LabCorp announced that its Covance Drug Development business will open a companion diagnostics lab in Morrisville, North Carolina. The facility also includes a genomics and molecular pathology lab to support clinical trials and diagnostic testing development, and houses manufacturing facilities for diagnostics materials and testing components.
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Emerging Biopharma and Rare Disease: Finding a Needle in a Haystack
Data-driven Patient Recruitment Solutions
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In anticipation of relocating, the EMA has started on the re-distribution of the workload relating to the evaluation and monitoring of medicines to ensure the quality of EMAs scientific assessments and compliance with legal timelines
Additionally, the EMA announced that the EU clinical trial portal and database’s go-live date has been postponed, due to technical issues with the IT systems.
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Talking the Patients' Language – the importance of effective, patient-centered engagement
On Demand
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Articles
This study looks at in-office conversations earlier in the patient journey toward a clinical trial, before suitable trial options have been identified or patient eligibility for a study has been established. These early conversations set the stage for patients’ understanding of and receptivity toward enrolling in a clinical trial in the future.
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Achieve Better Outcomes with New RBM Tech Enhancements
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