ACT

JUNE 25/2019


news roundup

Alzheimer's Study Adopts BYOD Model

Datacubed Health's app, platform and web-based portal will be used by scientists at the Dominantly Inherited Alzheimer Network (DIAN) at the Washington University School of Medicine in Saint Louis.


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Operational Challenges in Resourcing and
Executing Seasonal Infectious Diseases Studies

Europe: Thursday, June 27, 2019 at 3pm BST | 4pm CEST
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Phlexglobal Addresses New TMF Guidance from EMA

Phlexglobal announced an important industry advisory around the new European Medicines Agency guidance on Trial Master Files that took effect on June 6.


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Operational Challenges in Resourcing and Executing Seasonal Infectious Diseases Studies
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Unified Clinical Operations Survey Results Released

According to the Veeva 2019 Unified Clinical Operations Survey, there is an industrywide drive to streamline trial processes and systems for better study visibility and collaboration. Research from the survey finds that 100% of respondents surveyed report the need to improve information exchange among study partners.


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Operational Challenges in Resourcing and Executing Seasonal Infectious Diseases Studies
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Roche, IDDI Publish Data Around DFS in Breast Cancer

Commissioned by Roche Germany, IDDI has found data that suggests that it is appropriate to use disease-free survival as a surrogate for overall survival in trials in HER-2-positive breast cancer.


Articles

2018 FDA Approvals Examined

Ken Getz examines the 2018 FDA approvals with insights, saying "What is most notable about 2018's approval volume is not only the scientific innovations that produced them, but also where they originated, how they were funded, and the operating models, services, and technology solutions that supported them throughout the R&D process."


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COPD – Tackling the Unmet Needs
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Risk-Based Quality Management

To address the possibility of overlooked risk communication, a basic set of factors relevant to ensuring study quality should be identified for each study. Emphasis should be given to those factors that stand out as critical to study quality.

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In this edition

Large CROs Adapt to Emerging Biopharma
Unified Clinical Operations Survey Results Released
2018 FDA Approvals Examined

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Refocusing on Risk Mitigation in Starting Clinical Trials
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Blog Posts

Large CROs Adapt to Emerging Biopharma

In this interview, Chris Smyth, COO of IQVIA Biotech, discusses how large CROs are responding to EBP targets.


Separating Myth from Truth in Predicting Site Enrollment

Some investigator sites will recruit more patients than other sites. That tendency can prompt trial planners to set enrollment targets based on linear extrapolation – which is still the dominant thinking in our industry – as a means to identify and deploy the sites capable of enrolling the largest numbers of patients. The author suggests this thinking is a fallacy.



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Ask the editor

Lisa Henderson
Editor in Chief
LHenderson@mmhgroup.com

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Todd Baker
Group Publisher
TBaker@mmhgroup.com