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In this ISSUE

The Impact of Faster Drug Approvals on Oncology Clinical Trial Design

Regulatory Approval in India: An Updated Review

Virtual Clinical Trials: The Future of Patient Engagement?

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Industry Trends
Clinical Trials Confusing—Even to Doctors
Most physicians and many specialists have limited understanding of clinical trial data and research findings presented in prescription drug promotional materials for professional audiences.
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ERT Video Series
Check out the ERT video series, filmed on the show floor at DIA 2017, for interviews on Innovating Clinical Trial Management, eCOA in Clinical Research: Trends and Advances, and Optimizing Clinical Trial Imaging through Advanced Technology.
Click here to watch all 10 short videos
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Tomorrow's Clinical Trial, Powered by Modern EDC
See how to cut study build time in half, eliminate migrations, and remove the need for source data verification (SDV).
See a preview and watch the full webinar here.
Calendar
/ Interactive Response Technologies in Clinical Trials 2017 10/26-10/27 /
/ Data Privacy Summit for Life Sciences 10/30-10/31 /
/ Risk-Based Trial Management and Monitoring 2017 11/2-11/3 /
/ BioPharma Forum on Cannabis-Based Therapies 11/30-12/1 /
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Trial Materials
Overcoming Complexities of Clinical Trial Supplies in Latin America
Supply chain strategies require a close look at the regulatory factors and the drug import hurdles and hopes in the region.
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Exom Group is "The Human Digital CRO" , that provides value-added services through digital applications for clinical development of drugs & medical devices. We combine the strong medical, regulatory and operational expertise of our staff , with the most disruptive digital cloud and mobile solutions to reduce costs and increase quality and performance of Clinical Trials. We can manage studies in all Europe and USA. Learn more
mHealth
New mHealth Action Plan Released
The Duke Margolis Center for Health Policy (DMCHP) recently collaborated with the FDA to release an mHealth action plan entitled "Mobilizing mHealth Innovation for Real-World Evidence Generation."
... /Read more/
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Rare Diseases and the Eye - Envisioning Strategies for Success
Live Webcast: Friday, October 27 at 11:00am EDT
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Exclusive Interviews from the 2017 DIA Global Annual Meeting
Check out these exclusive interviews from the 2017 DIA Global Annual Meeting in Chicago, IL, conducted by the editors of Pharmaceutical Executive and Applied Clinical Trials. Whether or not you attended the event, here is your chance to gather insights from featured industry professionals.
Watch Videos

Ask the editor
Lisa Henderson
Editor in Chief
Lisa.Henderson@ubm.com

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Navigating the Regulatory Complexities of Orphan Drugs: Know the unwritten rules of designations and what's next
Live Webinar: Thursday, November 2 at 11:00am EDT
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Regulatory Authorities, FDA
FDA Moves to Broaden Acceptance of Real-World Evidence in Clinical Research
New legislation aims to expand regulatory acceptance of patient data from healthcare systems and observational studies.
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RBM Technology Impact on Clinical Roles: Centralized Monitoring is streamlining activities and changing roles across clinical development
On Demand
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Precision Medicine
The Success of Cell Therapies Will Depend on Automation
Automation will be key to improving efficiency and mitigating risk during the complex process of cell therapy production and delivery.
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Proactive Planning, a Transformational Revolution to Improving Clinical Trial Quality?
On Demand
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Future-proofing your Pharmacovigilance Delivery Model: Achieving scalability and cost effectiveness with AI/smart machines
Live Webinar: Wednesday, October 25 at 11:00am EDT
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Mike Tessalone
Publisher
Michael.Tessalone@ubm.com
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