news roundup
CRO SynteractHCR, and The GOG Foundation, a non-profit focused on gynecologic oncology research, will collaborate on a streamlined process for drug development companies to improve the timeliness of determining clinical research studies, and facilitate rapid trial execution in gynecologic oncology studies.
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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 |
Bracket, a clinical trial technology and specialty services provider, announced the release of CUBE™, an interactive response technology (IRT) solution. The solution leverages an iterative user acceptance build experience, which allows a UAT process that study teams can visualize during the kick off meeting.
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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 |
Chiltern has acquired Integrated Development Associates (IDA), a Japanese CRO specializing in integrating Japan and Asia into global drug development. Under this acquisition, IDA will do business as a subsidiary of Chiltern and be renamed IDA, a Chiltern Company.
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Capturing Continuous Glucose Monitoring Advantages
Live Webinar: Wednesday, June 28 at 11:00am EDT  Register now |
The Phase I Unit at Peking Union Medical College (PUMC) Hospital's Clinical Pharmacology Research Center (PUMCH-CPRC) in Beijing will employ Certara's Simcyp Population-based Simulator to develop physiologically-based pharmacokinetic (PBPK) models in support of Chinese new and generic drug applications to the Chinese Food and Drug Administration (CFDA).
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Emerging Biopharma and Rare Disease: Finding a Needle in a Haystack
Data-driven Patient Recruitment Solutions
Live Webinar: Thursday, June 8 at 2:00pm EDT
 Register now |
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Coming to terms with Patient Centricity
Live Webinar: Tuesday, June 20 at 12:00pm EDT
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Blog Posts
Listen to DIA executives discuss current trends in drug development, and the best way to optimize your time at the annual meeting in Chicago.
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Selecting and Auditing a Technology Vendor for Biopharmaceutical Development
Live Webcast: Thursday, June 8 at 11:00am EDT
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This article reports on industry trends from CBI's 3rd Annual Endpoint Adjudication Event, and will analyze the Endpoint Adjudication Survey results.
Payment automation solutions that are designed to optimize global research site performance and sustainability provide sponsors and CROs the ability to improve trial effectiveness by enabling more efficient, accurate and timely site payments and patient reimbursements around the world.
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Articles
Reasons to consider and how to implement an Enterprise Project Management Office (EPMO), to centralize coordination of all aspects of the projects in a pharmaceutical company.
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Achieve Better Outcomes with New RBM Tech Enhancements
Live Webinar: Wednesday, June 7 at 11:00am EDT
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This article looks at two emerging companies that use machine learning, artificial intelligence (AI) and neural networks to improve drug discover in the pharmaceutical sector.
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Talking the Patients' Language – the importance of effective, patient-centered engagement
Live Webinar: Tuesday, June 6 at 8:00am EDT
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