Veeda Picks ClinPhone CTMS
Operational Data Fights Cancer
A cancer-oriented CRO says ease of use and the ability to tailor payments were key factors in its choice.
Since time immemorial, sponsor firms have chosen software. Then it gets introduced, so to speak, to the throats of research sites. Sometimes principal investigators and clinical research associates (CRAs) like the technologies they are obliged to use. Sometimes they just use them. So it is remarkable that Greenphire has industry-savvy research sites knocking on its door with no mandate or funding from sponsors. Ten major academic medical centers (AMC) and a hundred independent clinical sites have called Greenphire and said, more or less, "we'd like to pay for your services with our own money." In a context of industry-sponsored trials, that's unheard of. Even small, independent Phase I units have taken the initiative to seek out Greenphire's solution and buy it on their own. Unified Approach ClinPage wrote about Greenphire more than two years ago, but the company's services and operations have since expanded. It launched a full-featured system to handle…more...
In the unofficial design manual for clinical trial software programs, there are numerous unwritten rules but only a single severe commandment. Any new solution must have exactly 52,009 powerful and essential…more...
While it supports a cottage industry of professionals, manually pushing piles of clinical trial data along from one system to the next isn't necessarily the most efficient way of doing things.…more...
Karen Hultberg was frustrated. The administrator of the New York Hospital Queens' Lang Research Center was trying to do more studies. But there was a big obstacle: for each research subject's…more...
One notable aspect of media coverage of clinical trials is the ready acceptance of the cost of a particular clinical research program. In every notable publication, as far as we can tell, the cost of a trial or a research program is confidently said to be so many tens or hundreds of millions of dollars. The amount…more...
One man's middle of nowhere is another man's perfectly situated. That's the way Paul Bishop and Lyle Camblos see Staunton, the small Virginia town that's home to their contract research organization (CRO), Atlantic Research Group (ARG). “It's equidistant from Rockville and RTP,” says Camblos, speaking of the myriad biotech companies along the I-270 corridor in Rockville, Md.,…more...
Even in 2009, in a context of clinical trials, "management" can mean just about anything. It may mean ... Karen, three cubicles away. Or a 5-year-old spreadsheet. Or a system that cost millions but sits unused. As a result, it's fair to say that clinical trial management systems (CTMS) do not enjoy a reputation for easy implementation,…more...
Want to get depressed? The Tufts Center For the Study of Drug Development has analyzed the length of clinical trials during two time periods: 1999-2002 and 2003-2006. The median number of days from first to last patient visit has doubled, to 598. Nineteen months. Can anyone think of any industry that takes twice as long to do…more...
A cancer-oriented CRO says ease of use and the ability to tailor payments were key factors in its choice.
IT departments like the new version of its Impact software, which now runs on a thumb drive.
ACS talks about a new product. The company is betting the combination of EDC and CTMS will appeal to biotech firms and contract research organizations.
Bayer’s Rob Musterer discusses why current clinical trial management systems aren’t serving the industry.
With impressive numbers, Pfizer’s Mike Collins talked about how the company is streamlining its clinical trial process.
In the third part of our series, a softer approach to win the hearts of clinician-investigators.
In the second segment of our series on investigator relationship management, Lilly discusses plans to zero in on high-performing sites.
Organizations
Conferences
Info & Opinion
© 2012 ClinPage. All Rights Reserved.