Life Sciences

Regulatory Report Tracking In Oracle Argus Safety

oracle-argus-safety-regulatory-report-tracking

 

Life Sciences - How Artificial Intelligence Can Enhance the Clinical Data Review and Cleaning Process
How Artificial Intelligence Can Enhance the Clinical Data Review and Cleaning Process

This guide analyzes how artificial intelligence – including machine learning – can be used by pharmaceutical and medical device companies to improve the clinical data review and cleansing process.

Get the Guide

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 down to various drafted/pending, submitted, or not submitted regulatory reports by destination. Based on your selection in the upper block, it dynamically displays the relevant reports from that regulatory authority on the lower part of the screen. 

The pharmacovigilance database allows for the comprehensive automation of worldwide reporting rules to be documented in the system, and then based on various case or event level attributes, fire one or more reports onto the screen. Our next Argus Safety feature-related blog post will cover this easy, yet comprehensive administration feature. To read past posts in our Argus Safety features series, click here.

In the meantime, if you’re interested in taking a closer look at Argus Safety, please contact us.

Leave a Reply

Your email address will not be published.

This site uses Akismet to reduce spam. Learn how your comment data is processed.

Rodney Lemery

Dr. Rodney Lemery specializes in the implementation, support, and development of software used in the collection, management, and analysis of clinical data. His accomplishments as director of safety and pharmacovigilance at Perficient include the management of numerous clinical application implementation projects. In addition to his expertise in clinical and safety applications, Rodney is able to navigate between the technical and clinical worlds with ease due to his complementary educational background in epidemiology. He also holds a part-time professorship in the School of Health Sciences at Walden University, which solidifies his ability to lead global safety implementations at Perficient. Rodney has been with Perficient, via the acquisition of BioPharm Systems, since 2000. Prior to joining the company, he worked at Pfizer.

More from this Author

Subscribe to the Weekly Blog Digest:

Sign Up
Follow Us
TwitterLinkedinFacebookYoutubeInstagram