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In our November/December issue:

FEATURED

Salary & Satisfaction: Industry Jobs Survey
We compare key findings from ACT and SCORR Marketing's new survey of clinical research professionals with overall workplace trends in the life sciences.

PEER-REVIEWED ARTICLES

What Sites Need Most
Michael J. Howley, Peter Malamis, Jim Kremidas
With site perspectives of clinical trial quality rarely heard, authors, using focus-group insights, present a statistical model for sponsors and CROs to identify the services and resources sites need to perform high-quality studies.
Trial 'Rescue' Guide
Pete Fronte, Beth Harper
Clinical trials that end up in "enrollment rescue mode" create major challenges for sponsors, CROs, and sites alike. Survey gleans important approaches that all three of these parties should consider when faced with rescue dilemmas.
Blockchain Boost for Supply Chain
Darryl G. Glover, Jan Hermans
Report examines how the use of blockchain technology can potentially impact clinical trial supply chains by improving the traceability of medicines, while enabling the gathering of patient-level data in a HIPAA-compliant manner.
NEWS

Washington Report: Jill Wechsler on FDA's efforts to smooth pathways for more transformative drugs—and hopeful new cures.

EU Report: Peter O'Donnell looks at the "what ifs" and "what might have been" in aftermath of EMA relocation announcement.

Global Report: Philip Ward details UK expert's take on ways to prevent clinical trial fraud.

Q&A: Discussion explores collaboration focused on using IT toolset to better manage clinical supplies and patient adherence.

DATA STANDARDIZATION: Updates, enhancements to CDISC's Glossary of Clinical Research Terminology unveiled.

CLINICAL TRIAL INSIGHTS

Real-World Data: Expanding Horizons
Ken Getz
Study spotlights the growing integration of real-world data and evidence in drug development and the remaining roadblocks to adoption.
CLOSING THOUGHT

Informed Consent's New Normal?
Darshan Kulkarni, Andrea Tunnard, Erin Grant
How a recent court ruling in Pennsylvania now requiring informed consent to be obtained by a medical doctor could have ripple effects throughout the U.S.

Download the
issue:
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BLOGS
Why We Should Talk to Patients Who Drop Out of Clinical Trials
FDA Seeks More Effective Clinical Research Oversight
Introspective Approaches Towards Issues Resolution
WEBCAST
The Benefits of a Data-driven Approach to Feasibility
Learn how data-driven feasibility may be an answer to today's drug development challenges, by connecting the most relevant patient, site, and investigator data with analytic tools and targeted processes.

If you would like to submit an article to Applied Clinical Trials, contact Lisa Henderson, Editorial Director - [email protected]

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