Posts Tagged ‘InForm’

She Has Great Ideas

An Opportunity to Get Your Clinical One Questions Answered

Through our upcoming fireside chat with Perficient’s Mike Grossman, GM, Life Sciences, and Oracle’s Jim Streeter, Global VP, Life Sciences Product Strategy, we are really aiming to clarify some fundamental questions relating to Oracle’s Clinical One and what this platform approach could mean for our clients.  They are going to get right back to the basics of why it is beneficial to invest […]

[Invitation] Clinical One Fireside Chat with Oracle’s Global VP of Life Sciences Product Strategy

Over the last couple of years, Oracle has been incredibly hard at work developing, from the ground up, what many are calling a game-changer for Oracle—and its customers. It’s called Clinical One. If your company uses any Oracle Health Sciences applications, you’ve probably already heard a little about Clinical One. You may already have received […]

InForm

Improving the Performance of Oracle InForm Reports

I recently shared a project in which we helped a pharmaceutical company build studies in Oracle InForm. Today, I want to share a project that has to do with the length of time it took for a major pharmaceutical company to run Oracle InForm reports, which caused significant problems, including delays in being able to […]

InForm

Oracle InForm Study Building

The beauty of having a versatile team of clinical data management experts is that they understand the life sciences industry and how companies operate. Through client projects and having worked at pharma companies in previous roles, they know the many unique challenges and needs of pharmaceutical and medical device companies. Equally important, they’re also technologists. […]

[Webinar] An Intro To Clinical Study Migrations

Migrating clinical studies from one database to another (such as Oracle Clinical to Oracle Clinical or Oracle Clinical to Oracle InForm or Medidata Rave), is a complex process that requires a thorough understanding of clinical data management, technology, and the regulations that govern clinical trials. Join me and my colleague, Richard Gavan, for an informational webinar […]

Oh My, Where Has The Time Gone?

Next week, we are exhibiting at Oracle Industry Connect (OIC) 2017 in Orlando, Florida. For those not familiar with OIC, it is a conference dedicated to a variety of verticals, including Life Sciences and Healthcare. Prior to the existence of OIC, the Annual Oracle Health Sciences User Group (OHSUG) Meeting was an event devoted to users […]

Identifying Which Data To Review During A Clinical Data Review

In my last blog post, I presented some thoughts on showing data changed since last review. Today, we will concentrate on the level of scrutiny and what happens when recording the user actions in the review. Not all data may require the same level of scrutiny during a review. Additional focus may need to be […]

Identifying New Or Changed Data During A Clinical Data Review

In my previous post, we discussed some examples of business rules that might be applied depending on how many people are performing a clinical data review. Today, we’ll discuss approaches for selecting the data that is being reviewed. In any data review that occurs multiple times during the course of a study there are two […]

Reviewing Clinical Data With Value Added And External Data

In my last post, I discussed performing a clinical data review in Oracle’s Data Management Workbench, which takes value added data into consideration. Today, we’ll take it a step further and add external data into the mix. This scenario extends the data available for review by including data from external partners who may be managing […]

4 Ways You Can Improve The Clinical Data Review Process

In my previous blog post entitled Using On-demand Data With Dynamic Data Writeback In Spotfire, I discussed using Spotfire as an aid for Clinical Review of data along with supporting writeback capabilities to record the user review actions.  As a follow-on discussion, I wanted to expand those capabilities to include Clinical Data Cleaning Review in […]

Pfizer Says “Yes” To Oracle

Very good news out of Oracle this week. After a thorough review of solutions on the market, Pfizer chose to implement what can essentially be seen as Oracle’s complete suite of clinical and drug safety applications. This doesn’t necessarily come as a surprise, since the pharma company has been a long-time user of Oracle’s legacy […]

Answers To Questions From Risk-Based Monitoring (RBM) Webinar

  On January 14, 2016, Perficient hosted a webinar titled Leveraging Siebel CTMS for Risk-Based Monitoring. We received some good questions during the webinar and figured we’d share them (and the answers) with you. 

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