Organizations
Conferences
Info & Opinion
October 7, 2008
Using genomic expertise, the Almac Group starts a search for its own compounds.
Four clinical organizations in Massachusetts have come together to help regions that want to get more of the global medical research pie.
In Side Effects, reporter Alison Bass delves into the New York Attorney General’s 2004 case against GlaxoSmithKline.
The SAFE-Biopharma Association is hoping to nudge the pharmaceutical industry toward a single electronic signature standard.
Does Windows have something to contribute to the clinical trial arena? Microsoft asserts its platform is more open and robust.
Even in a global clinical trial, driven by 21st century medicinal chemistry, gene arrays and relational databases, there is a medieval component. A stubborn one. Thousands of pieces of paper, each with a squiggle at the bottom. Signatures. John Hancocks. Squiggles mean the paper has to be pushed like sausage… more...
Microsoft Word documents and Excel spreadsheets are as ubiquitous in the life sciences as in any other industry. In the clinical trial space, the question is: does having trial-related data in non-compliant, non-validated applications present an opportunity or a risk? Can Microsoft programs co-exist or support clinical-trial-specific applications? Or should… more...
The 2008 Drug Information Association (DIA) annual meeting featured a painful session on metrics in clinical trials. Not painful because of any of the speakers, who were polished and insightful. No, it was painful because sizable clinical research projects and sophisticated companies are not really being managed. We’re using the… more...
After PharmaNet‘s (Nasdaq: PDGI) first quarter news that it had again lost $30 million in contracts—the same thing happened to the company in the last quarter of 2007—Standard and Poor’s (S&P’s) revised its outlook on the contract research organization (CRO) from stable to negative. It wasn’t just the loss of… more...
Every two weeks or so, Tim Schroeder gets a call from a fund manager or private equity group wanting to buy Clinical Trials and Consulting Services , the liver and transplant-focused contract research organization (CRO) he founded in Cincinnati almost a decade ago. “They say, ‘Hey, we want to buy… more...
Is there a more wasteful federal program than NASA? Does it matter if a robot can land on some planet and take a picture of itself digging a small hole? It’s clear that NASA is both useless and popular. Which is the opposite of the pharmaceutical industry: indispensible and unpopular.… more...
Independent accreditation in the clinical research world had been slow to catch on, but now it suddenly appears to be a topic of high interest. Compliance with existing regulations is not enough, it seems. Just take the numbers. In its first seven years of accrediting those in clinical research, the… more...
Shouldn’t every protocol be “smart”? It may seem like a rhetorical question. How much of the clinical trial data and budget are truly necessary? Are there ways to simplify the process? As Genentech’s Paul Clarkson, director of data management, explains in today’s podcast, some companies rush to put too much… more...
There are not enough minorities, seniors and children included in trials of drugs for minorities, seniors and children. That’s simply bad for society and industry. That’s one of the main thrusts of the Eliminating Disparities in Clinical Trials (EDICT) report, released recently by researchers at Baylor College of Medicine in… more...
They were going to the same meetings. Seeing each other in the same airports. Bidding on the same projects. One thing lead to another. Then, just yesterday, ClinPhone and invivodata announced a global marketing alliance for electronic patient-reported outcomes. The press release is here. It’s the latest sign that the… more...