Fewer Features & Faster Setup
EDC, CTMS for Biotechs From ACS
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.
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 features. Why? So that experts and consultants in the pharmaceutical industry can stand back and exclaim, "Wow! You have precisely the 52,009 features that we require you to have." A San Francisco entrepreneur named Jae Chung is planning to to disregard that commandment with a company called GoBalto. Chung is no dreamy software architect. A 40-something ex-McKinsey consultant, he founded and sold Celltrion, a Korean biotechnology firm that specializes in contract manufacturing and generics. Chung has sufficient resources to keep GoBalto in the hunt against traditional, established clinical trial management system (CTMS) and document management suppliers that include Oracle, Parexel, SAS, Study Manager, Clinical Force, BioClinica, Intralinks and Mission3. Chung becomes uneasy when his system is compared to a traditional,…more...
In 2011, with electronic data capture (EDC) systems in broad usage, there is only one deep question about the technology that remains. To wit: should EDC be confined to merely gather…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…more...
“Give us the tools and we will finish the job,” Winston Churchill wrote to a friend. The year: 1941. World War II was just getting started. In 2009, thousands of web-based…more...
Is the word “eclinical” meaningless jargon? A good way for people to pay lip service to the future without actually building it? The people at Medidata Solutions have been trying to lend some definitional and operational clarity to what “eclinical” means. Two months ago, they announced Developer Central, a set of standards to facilitate the connection of…more...
For the contract research organization (CRO) serving multiple clients, it can be tough to stay abreast of multiple projects all over the world. In many ways, the technology advances of the past few years have made this more onerous, not less. The sheer number of systems with vital data continues to grow. Veeda Oncology is hoping to…more...
We were looking around for how many USB, or “thumb” drives are sold every year. Alas, we could locate no statistics. We canUSB…more...
There is scarcely a more tired phrase than “it’s not rocket science.” But what if electronic data capture were conceived as something that had to be as robust as the software to protect astronauts or Navy pilots? That seems to be the approach of Prelude Dynamics, a Texas startup with more than a dozen employees and active…more...
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.
Discussing its recent quarterly earnings, Parexel is optimistic on all fronts.
Wrestling with the surge in disparate types of systems in the clinical trial arena, PharmaPros combines services and software.
With appeal for academia and federally sponsored trials, the North Carolina firm has a solution that combines tools for collecting data and managing trials.
With a new version of its web-based electronic data capture solution, TrialStat emphasizes reports that can easily be generated for all stakeholders in the clinical trial process.
Jane Clarke discusses what Wyeth has done and where it’s going with electronic data capture, which is shaping up to be a crucial element of the company’s clinical development plan.
Some customers invest in a clinical trial management system for better visibility into a trial. Others like owning their data for future projects.
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