Posts Tagged ‘CTMS’

  Last month, Perficient attended the Oracle OpenWorld conference and presented at several sessions. One of those sessions was on how clinical trial management systems (CTMS) can support risk-based monitoring (RBM) strategies at life sciences companies. 

  Param Singh, the director of Perficient’s clinical operations solutions team, was just presented with one of Perficient’s highest internal awards for leadership. The Soaring Eagle award recognizes leaders who rise to their own personal heights while inspiring others to do the same through support, encouragement, and the creation of opportunities for professional and career […]

  Over the last decade, the life sciences industry has gone from running clinical trials on paper or, in many cases, in Excel, to leveraging comprehensive web-based systems, such as electronic data capture (EDC) and clinical trial management systems (CTMS). But, in more recent years, the widespread use of mobile technology has enabled even more […]

  Ed Miseta, Chief Editor of Clinical Leader, recently interviewed Mike McKay, Associate Director of Operational Excellence for Shire Pharmaceuticals, on his view of the clinical IT space and how it’s affecting his company. Here are several takeaways from his interview: 

  Let’s face it, anything with “99+” in the title is catchy. That’s why we used it for our upcoming 99+ Siebel CTMS Best Practices You Should Follow webinar. We wanted you to know how content-rich the webinar will be, whether you’re a current user of Oracle’s clinical trial management system (CTMS) or in the […]

  As long as you have the experience listed in the job descriptions. But, to put it simply, if you’ve worked in the life sciences industry, you’re already ahead of the game. Check out the job openings we have on our life sciences team and apply if you’re interested. We’ll keep your application secret. Promise. […]

  Perficient’s Life Sciences practice regularly monitors the software release notes for several Oracle Health Sciences applications, as well as our own clinical and safety systems. The systems covered in our review are: 

  On Thursday, April 23, 2015, we delivered a webinar on 21 CFR Part 11, based on a recent blog series. During the Q&A session at the end, someone asked the following question: Does 21 CFR 11 apply to a CTMS (clinical trial management system), CDMS (clinical data management system), EMR (electronic medical record), or […]

  In our last “cloud fact or fiction” post, we discussed integrating systems that are deployed in the cloud. This week, let’s talk about system administration. Claim #8: Choosing a hosted clinical or safety system means relying on the vendor for system administration tasks. 

  I recently stumbled upon the picture on the right on LinkedIn and it reminded me of a conversation that I had with my mother, who is an architect by trade. She told me that many roads came to be what they are today, not by well-thought-out plans, but rather by people and animals getting […]

  Managing the investigational product lifecycle can be difficult without a system designed specifically for that function. It is a complex process with high stakes – one wrong move can halt a study, put subjects at risk, or open up a sponsor for a compliance audit. The struggle is that product tracking systems can be […]

  It’s no secret that having a clinical trial management system (CTMS) streamlines and simplifies the running of clinical trials, and that Oracle’s Siebel Clinical (Siebel CTMS) is the most robust system in the space. But, as a Study Manager, what you might not know is exactly how it would make YOUR work life easier. […]