Posts Tagged ‘adverse event reporting system’

Hi everyone, it’s Indy here. For those of you who may not recognize my name, I’ve been helping lead our Argus Safety installations for the past few years. I wanted to drop a quick note to personally invite you to the webinar I’ll be presenting next week. It’ll be relatively short, by design, but it […]

Now that July is here, I thought it would be neat to look back at what our readers found most interesting last month. Below are the top five blog posts Perficient’s life sciences practice wrote in June – they’re ranked in order of popularity, with number one being the most viewed piece. What Exactly Is An “Adverse […]

When I’m approached by clients to discuss safety projects, it is generally about implementing Oracle’s Argus Safety, upgrading the system, or discussing their ability to comply with regulatory requirements. Recently, I was asked about migrating from a legacy drug safety database to Argus. We discussed the methods available, such as leveraging an Oracle dump, a […]

Now that June is here, I thought it would be neat to look back at what our readers found most interesting last month. Below are the top five blog posts Perficient’s life sciences practice wrote in May – they’re ranked in order of popularity, with number one being the most viewed piece. How To Import Data Into Siebel […]

Bring out the popcorn! This Thursday, Dr. Rodney Lemery, one of our experts in drug safety and pharmacovigilance, will be delivering a webinar on the latest version of Oracle Argus Safety, the most widely used and trusted PV system on the market. This presentation is meant for everyone, whether you’re already using the system and […]

  An interesting thing happened in pharma and investing. It involved Regeneron and their July 24, 2015 FDA-approved cholesterol drug, Praluent. Forbes outlined the situation, which caused Regeneron stock to drop significantly, in a January 6, 2016 article. According to Matthew Herper, a Forbes columnist, investors got a hold of data from the FDA’s Adverse […]

Code list maintenance is critical in Oracle’s Argus Safety. These code lists often present as drop-downs in the case entry sub-system. While the entry, modification or removal of these list of value options are very convenient, it does take some effort to ensure the reliable data points that are used everywhere in the system are […]

  We recently discussed the ability to access previously visited adverse event cases very quickly in Oracle’s safety and pharmacovigilance system, Argus Safety. For this post, we’ll cover a feature that many of our clients love. Argus Safety enables users to open multiple cases simultaneously, although it’s not possible to view both of the cases at […]

  We recently discussed reporting and the tracking of E2B transmissions in Oracle Argus Safety. Today, we’ll highlight some of the dashboards that are available in the drug safety and pharmacovigilance system. As you can see from the menu in the first screenshot below, these are the dashboards built into the system. 

  When it comes to periodic reporting, we feel that the generation and tracking of periodic reports in Oracle’s Argus Safety is far easier than in other safety and pharmacovigilance systems. In the system, periodic reports are all created and generated from a central screen within the application.   The four basic kinds of periodic […]

  I was recently listening to the radio and heard about a book “Who Knew?: Things You Didn’t Know About Things You Know Well” and it reminded me of a story that that our safety and pharmacovigilance director, Dr. Rodney Lemery, told during a webinar earlier this year. Where did the name Argus Safety come […]

  One of the things we hear most is how simple Oracle Argus Safety is to navigate. In the image (click it to enlarge) above, you’ll notice a familiar folder structure in the upper part of the Regulatory Reports screen – it looks just like Windows Explorer and works similarly. It allows you to drill […]