Can a large pharma build a clinical data reporting system that employees will actually clamor to use? Wait. Back up. What is the ultimate objective for any system for clinical trial data? Is it to make a dramatic investment in something new (software) that embalms something old (a sea of…more...
How does the FDA want sponsors to handle patient-reported outcome data? That question is looming over every company that ponders whether a paper diary or some other approach is warranted. PHT offered a webinar on patient reported outcomes (PRO) just a few weeks ago that we regret to have missed.…more...
December 3, 2008
Consultant Ron Waife of Waife & Associates discusses what eclinical means and why it matters.
The conference industry should borrow an idea from the medical journals, our guest author says.
Lilly discusses how data management is changing in the era of electronic data capture.
Moving work to India is not just about cost, says Bristol Myers. It’s about performance and quality too.
A report from the Clinical Trials Congress about risk. One message: start a regulatory conversation early. And consult your preclinical team.
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