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Agile Product Development Methodology holds great promise for use in Adaptive Clinical Study Development.

Despite the evidence that the Hispanic population is increasing at a formidable rate, they not only face disadvantages in health care access, but are significantly underrepresented as participants in biomedical research.

These three steps should take place in order to ensure an optimal site selection.

Cancer immunotherapies require different standards for evaluating their safety and effectiveness. Understanding these standards-and the other major challenges of immuno-oncology studies-is critical to drug development success.

The topic of clinical trial quality and compliance continues to evolve in clinical operations, based on discussions at ExL’s 9th Proactive GCP Compliance Conference.

How the Clinical Development Design (CDD) Framework can offer repeatable, reusable clinical designs based on "enabling information."

In this interview, Kevin Hudziak will expand on Lilly’s initiatives to change the face of clinical trials through patient engagement and education initiatives.

Jill Wechsler on the tug of war in accelerating orphan drug development.

Relocating the European Medicines Agency was always going to be hard-but no-one ever expected it to degenerate into farce.

The use of natural history (NH) studies early in clinical research can help facilitate development programs for orphan drugs.

Lisa Henderson discusses randomized clinical trials with active and non-active placebo treatments.

Click the title above to open the Applied Clinical Trials April 2018 issue in an interactive PDF format.