Development

Advanced Planning

Although the European and American approaches to pharmaceutical risk management differ slightly, both share the common objective of ensuring patient safety for marketed products.

Streamlining Safety Data

With electronic data collection becoming more mainstream, clinical trialists are now looking to incorporate safety data into the electronic mix as well.

Image Awareness

Radiological biomarkers hold the potential to be a positive force in pharmaceutical research, but the adoption of imaging techniques as a useful tool for drug development has been slow to materialize.

Control Mechanism

A rapidly increasing rate of type 2 diabetes has researchers scrambling for new interventions to combat the chronic condition.

BIOspeak

Jim Greenwood, president and CEO of the Biotechnology Industry Organization (BIO) and a former member of the U.S. Congress, discusses the most critical policy challenges facing the industry today.

Asian Migration

Access to patients, lower costs and increased efficiencies are leading to an explosion in the amount of clinical research being conducted in Asia.

Joining Forces

Global partnerships enable big pharma to streamline drug development and refocus their efforts on core competencies.

The State of Stents

Drug-eluting stents have been under fire recently, but the medical community has yet to decide if the risks outweigh the rewards.

Culture Shift

Drug safety monitoring needs to begin early in the development process and continue throughout the product’s entire lifecycle.

A New Era Dawns

As the march toward universal electronic submission of regulatory documents continues, regulators and pharmaceutical manufacturers are learning how to best implement the new technology.

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After decades of neglect, leading to a rapid increase in incidence, tuberculosis started gaining attention from industrialized nations over the past 10 years. With this new focus, TB’s incidence has started to decrease—but barely.

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